Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556.

Authors

Edmund S Cauley, George Washington University
Ahlam Hamed
Inaam N Mohamed
Maha Elseed
Samantha Martinez, George Washington University
Ashraf Yahia
Fatima Abozar
Rayan Abubakr
Mahmoud Koko
Liena Elsayed
Xianhua Piao
Mustafa A Salih
M Chiara Manzini, George Washington University

Document Type

Journal Article

Publication Date

4-13-2019

Journal

Neurogenetics

DOI

10.1007/s10048-019-00577-2

Comments

Epub ahead of print

APA Citation

Cauley, E., Hamed, A., Mohamed, I., Elseed, M., Martinez, S., Yahia, A., Abozar, F., Abubakr, R., Koko, M., Elsayed, L., Piao, X., Salih, M., & Manzini, M. (2019). Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556.. Neurogenetics, (). http://dx.doi.org/10.1007/s10048-019-00577-2

Peer Reviewed

1