The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non‐syndromic mental retardation

BACKGROUND: The molecular basis of autosomal recessive non‐syndromic mental retardation (NSMR) is poorly understood, mostly owing to heterogeneity and absence of clinical criteria for grouping families for linkage analysis. Only two autosomal genes, the PRSS12 gene on chromosome 4q26 and the CRBN on...

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Detalhes bibliográficos
Main Authors: Basel‐Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2006
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2563235/
https://ncbi.nlm.nih.gov/pubmed/16033914
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.035709
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