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Familial cosegregation of rare genetic variants with disease in complex disorders

Family-based designs are increasingly being used for identification of rare variants in complex disorders. This paper addresses two questions related to the utility of these designs. First, under what circumstances are rare disease-related variants expected to cosegregate with disease in families? S...

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Bibliografski detalji
Glavni autori: Helbig, Ingo, Hodge, Susan E, Ottman, Ruth
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 2013
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3598309/
https://ncbi.nlm.nih.gov/pubmed/23010752
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.194
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