Incorporating epilepsy genetics into clinical practice: a 360°evaluation
Genetic screening: actionable information for epilepsy patients and clinicians Screening for epilepsy-related gene variants can lead to effective, personalized treatment plans while reducing costs. UK and Danish scientists, led by Deb Pal, King’s College London, evaluated a new service within the UK...
Enregistré dans:
Auteurs principaux: | Stephanie Oates, Shan Tang, Richard Rosch, Rosalie Lear, Elaine F. Hughes, Ruth E. Williams, Line H. G. Larsen, Qin Hao, Hans Atli Dahl, Rikke S. Møller, Deb K. Pal |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2018
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/fd1d22dfee3c4f5984bcd5e51f0e638b |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function
par: Laura B. Jones, et autres
Publié: (2021) -
A Bayesian network approach incorporating imputation of missing data enables exploratory analysis of complex causal biological relationships.
par: Richard Howey, et autres
Publié: (2021) -
Acta Nº360
par: Banco Central de Chile
Publié: (2019) -
Transcriptome Analysis Reveals Higher Levels of Mobile Element-Associated Abnormal Gene Transcripts in Temporal Lobe Epilepsy Patients
par: Kai Hu, et autres
Publié: (2021) -
Incorporating Screencasts In Online Teaching
par: Elaine Peterson
Publié: (2007)