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
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