Long-read single molecule real-time (SMRT) sequencing of GBA1 locus in Gaucher disease national cohort from Argentina reveals high frequency of complex allele underlying severe skeletal phenotypes: Collaborative study from the Argentine Group for Diagnosis and Treatment of Gaucher Disease

Gaucher disease is reckoned for extreme phenotypic diversity that does not show consistent genotype/phenotype correlations. In Argentina, a national collaborative group, Grupo Argentino de Diagnóstico y Tratamiento de la Enfermedad de Gaucher, GADTEG, have delineated uniformly severe type 1 Gaucher...

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Autores principales:	G. Drelichman, N. Fernández Escobar, B. Soberon, N. Basack, J. Frabasil, A. Schenone, G. Aguilar, M. Larroudé, J. Knight, D. Zhao, J. Ruan, P.K. Mistry
Formato:	article
Lenguaje:	EN
Publicado:	Elsevier 2021
Materias:	Gaucher disease Bone disease Mutation analysis Genotype phenotype correlation Medicine (General) R5-920 Biology (General) QH301-705.5
Acceso en línea:	https://doaj.org/article/98b4f2892f6c4590959c830cdc82cef0
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Long-read single molecule real-time (SMRT) sequencing of GBA1 locus in Gaucher disease national cohort from Argentina reveals high frequency of complex allele underlying severe skeletal phenotypes: Collaborative study from the Argentine Group for Diagnosis and Treatment of Gaucher Disease

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