Molecular genetics of human primary microcephaly: an overview
Molecular genetics of human primary microcephaly: an overview
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
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 decrease in size. MCPH is a neurogenic mitotic disorder,...
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Full title
Molecular genetics of human primary microcephaly: an overview
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4315316
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4315316
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ISSN
1755-8794
E-ISSN
1755-8794
DOI
10.1186/1755-8794-8-S1-S4
