Male hypogonadism caused by a homozygous missense mutation of the LHB gene

QR Code

Male hypogonadism caused by a homozygous missense mutation of the LHB gene

Saved in:

Bibliographic Details
Main Authors:	Jie Chen, Wen-ting Yi, Yuan-Qing Cui, Wen-ting Wang, Xiong Wang
Format:	article
Language:	EN
Published:	The Korean Association of Internal Medicine 2021
Subjects:	Medicine R
Online Access:	https://doaj.org/article/609e4dcbd68e4412b817f0a91f4364c2
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Biomarkers of male hypogonadism in childhood and adolescence
by: Rey Rodolfo A.
Published: (2020)

Missense Mutations of Codon 116 in the SOD1 Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype
by: Xinmei Wen, et al.
Published: (2021)

Safety and efficacy of testosterone gel in the treatment of male hypogonadism
by: Kishore M Lakshman, et al.
Published: (2009)

Decoding disease-causing mechanisms of missense mutations from supramolecular structures
by: Atsushi Hijikata, et al.
Published: (2017)

Whole Exome Sequencing Identifies a Novel Homozygous Missense Mutation in the CSB Protein-Encoding <i>ERCC6</i> Gene in a Taiwanese Boy with Cockayne Syndrome
by: Ching-Ming Lin, et al.
Published: (2021)

Testosterone depot injection in male hypogonadism: a critical appraisal
by: Aksam A Yassin, et al.
Published: (2008)

A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts
by: Yuyan You, et al.
Published: (2021)

A MISSENSE MUTATION OF MSX1 GENE IN PAKISTANI FAMILIES WITH HYPODONTIA
by: Muhammad Nawaz, et al.
Published: (2019)

R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
by: Luigi Maione, et al.
Published: (2013)

A homozygous mutation in the stem II domain of RNU4ATAC causes typical Roifman syndrome
by: Yael Dinur Schejter, et al.
Published: (2017)

A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease
by: Gudny A. Arnadottir, et al.
Published: (2018)

Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis
by: Johanna Tommiska, et al.
Published: (2017)

Guidelines for the diagnosis and treatment of testosterone deficiency (hypogonadism) in male patients with diabetes mellitus (Draft)
by: Galina Afanas'evna Melnichenko, et al.
Published: (2017)

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
by: Najim Lahrouchi, et al.
Published: (2019)

A homozygous R148W mutation in Semaphorin 7A causes progressive familial intrahepatic cholestasis
by: Qiong Pan, et al.
Published: (2021)

A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy.
by: Tommaso Pippucci, et al.
Published: (2013)

A homozygous nonsense mutation in DCBLD2 is a candidate cause of developmental delay, dysmorphic features and restrictive cardiomyopathy
by: Kheloud M. Alhamoudi, et al.
Published: (2021)

Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy
by: Grażyna T. Truszkowska, et al.
Published: (2017)

Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations.
by: Bruno Francou, et al.
Published: (2011)

PremPLI: a machine learning model for predicting the effects of missense mutations on protein-ligand interactions
by: Tingting Sun, et al.
Published: (2021)

Rimklb mutation causes male infertility in mice
by: Koji Maekura, et al.
Published: (2021)

The Mechanisms and Management of Age-Related Oxidative Stress in Male Hypogonadism Associated with Non-communicable Chronic Disease
by: Kristian Leisegang, et al.
Published: (2021)

Can Low SHBG Serum Concentration Be A Good Early Marker Of Male Hypogonadism In Metabolic Syndrome?
by: Jarecki P, et al.
Published: (2019)

Drug resistance missense mutations in cancer are subject to evolutionary constraints.
by: Ran Friedman
Published: (2013)

Homozygous duplication identified by whole genome sequencing causes LRBA deficiency
by: Daniele Merico, et al.
Published: (2021)

Missense mutation of VKORC1 leads to medial arterial calcification in rats
by: Arnaud Michaux, et al.
Published: (2018)

Avoiding dangerous missense: thermophiles display especially low mutation rates.
by: John W Drake
Published: (2009)

Whole-exome sequencing reveals a novel homozygous mutation in the COQ8B gene associated with nephrotic syndrome
by: Mohd Fareed, et al.
Published: (2021)

Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene.
by: Doreen Becker, et al.
Published: (2010)

Age-related hypogonadism in men with metabolic syndrome
by: Yulia Alexandrovna Tishova, et al.
Published: (2010)

Primary hypothyroidism as a predictor of the hypogonadism development
by: N.V. Pasyechko, et al.
Published: (2021)

Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene
by: Xiaona Luo, et al.
Published: (2021)

A novel missense mutation of the NAT10 gene in a juvenile Schnauzer dog with chronic respiratory tract infections
by: Barry A. Hedgespeth, et al.
Published: (2021)

Missense mutation in selenocysteine synthase causes cardio-respiratory failure and perinatal death in mice which can be compensated by selenium-independent GPX4
by: Noelia Fradejas-Villar, et al.
Published: (2021)

Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment
by: Bingbo Zhou, et al.
Published: (2021)

A structural systems biology approach for quantifying the systemic consequences of missense mutations in proteins.
by: Tammy M K Cheng, et al.
Published: (2012)

Exome sequencing and functional analysis identifies a novel mutation in EXT1 gene that causes multiple osteochondromas.
by: Feng Zhang, et al.
Published: (2013)

Cognitive effects of testosterone and finasteride administration in older hypogonadal men
by: Borst SE, et al.
Published: (2014)

Mutations in COMP cause familial carpal tunnel syndrome
by: Chunyu Li, et al.
Published: (2020)

Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
by: Mayuko Tamura, et al.
Published: (2017)