A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.

Naseer, Muhammad Imran

A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family. [electronic resource] - Annals of Saudi medicine - 148-153 p. digital

Publication Type: Case Reports; Journal Article

0975-4466

10.5144/0256-4947.2017.148 doi


Amino Acid Substitution
Cell Cycle Proteins
Child
Consanguinity
Cross-Sectional Studies
Exome--genetics
Female
Humans
Intellectual Disability--genetics
Male
Microcephaly--genetics
Mutation, Missense
Nerve Tissue Proteins--genetics
Saudi Arabia
Young Adult