Back to search

Article

Case Report: Two Cases of Autosomal Recessive Primary Microcephaly Caused by WDR62 Gene Mutation

2022-04-04

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Autosomal recessive primary microcephaly (MCPH) is a rare genetic disease characterized by a reduction in head circumference at birth and intellectual disability with or without structural abnormalities of the brain. Due to the heterogeneity of its phenotype, we cannot effectively predict the severity of its clinical manifestations at present, which is also a si...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
218f5760-fc1e-5082-af2a-e7d37b9f6f16
DOI
10.21203/rs.3.rs-1388753/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Case Report: Two Cases of Autosomal Recessive Primary Microcephaly Caused by WDR62 Gene MutationDOI 10.21203/rs.3.rs-1388753/v1
Select a neighboring publication to make it the new centre.