TY  - GEN
AU  - Naseer,Muhammad Imran
AU  - Rasool,Mahmood
AU  - Sogaty,Sameera
AU  - Chaudhary,Rukhaa Adeel
AU  - Mansour,Haifa Mansour
AU  - Chaudhary,Adeel G
AU  - Abuzenadah,Adel M
AU  - Al-Qahtani,Mohammad H
TI  - A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family
SN  - 0975-4466
PY  - 2017///0707
KW  - Amino Acid Substitution
KW  - Cell Cycle Proteins
KW  - Child
KW  - Consanguinity
KW  - Cross-Sectional Studies
KW  - Exome
KW  - genetics
KW  - Female
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Microcephaly
KW  - Mutation, Missense
KW  - Nerve Tissue Proteins
KW  - Saudi Arabia
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.5144/0256-4947.2017.148
ER  -