The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome

BACKGROUND: Despite remarkable advances in genetic testing, many adults with syndromic epilepsy remain without a molecular diagnosis. The challenge in providing genetic testing for this patient population lies in the extensive genetic heterogeneity associated with epilepsy. Even for the subset of ep...

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Detalles Bibliográficos
Main Authors: McDonell, Laura M, Warman Chardon, Jodi, Schwartzentruber, Jeremy, Foster, Denise, Beaulieu, Chandree L, Majewski, Jacek, Bulman, Dennis E, Boycott, Kym M
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2014
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3916514/
https://ncbi.nlm.nih.gov/pubmed/24479948
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-14-22
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