Molecular genetics of human primary microcephaly: an overview

Autosomal recessive primary microcephaly (MCPH) is a neurodevelopmental disorder that is characterised by microcephaly present at birth and non-progressive mental retardation. Microcephaly is the outcome of a smaller but architecturally normal brain; the cerebral cortex exhibits a significant decrea...

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Dettagli Bibliografici
Pubblicato in:BMC Med Genomics
Autori principali: Faheem, Muhammad, Naseer, Muhammad Imran, Rasool, Mahmood, Chaudhary, Adeel G, Kumosani, Taha A, Ilyas, Asad Muhammad, Pushparaj, Peter Natesan, Ahmed, Farid, Algahtani, Hussain A, Al-Qahtani, Mohammad H, Saleh Jamal, Hasan
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2015
Soggetti:
Review
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4315316/
https://ncbi.nlm.nih.gov/pubmed/25951892
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8794-8-S1-S4
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