Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

BACKGROUND: Autosomal recessive primary microcephaly is a disorder of neurogenic mitosis that causes reduction in brain size. It is a rare heterogeneous condition with seven causative genes reported to date. Mutations in WD repeat protein 62 are associated with autosomal recessive primary microcepha...

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Detalles Bibliográficos
Autores principales: Kousar, Rizwana, Hassan, Muhammad Jawad, Khan, Bushra, Basit, Sulman, Mahmood, Saqib, Mir, Asif, Ahmad, Wasim, Ansar, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196702/
https://www.ncbi.nlm.nih.gov/pubmed/21961505
http://dx.doi.org/10.1186/1471-2377-11-119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196702/
https://www.ncbi.nlm.nih.gov/pubmed/21961505
http://dx.doi.org/10.1186/1471-2377-11-119

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