APA

Naseer M. I., Rasool M., Jan M. M., Chaudhary A. G., Pushparaj P. N., Abuzenadah A. M. & Al-Qahtani M. H. (20170526). A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family. : Journal of the neurological sciences.

Chicago

Naseer Muhammad Imran, Rasool Mahmood, Jan Mohammed M, Chaudhary Adeel G, Pushparaj Peter Natesan, Abuzenadah Adel M and Al-Qahtani Mohammad H. 20170526. A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family. : Journal of the neurological sciences.

Harvard

Naseer M. I., Rasool M., Jan M. M., Chaudhary A. G., Pushparaj P. N., Abuzenadah A. M. and Al-Qahtani M. H. (20170526). A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family. : Journal of the neurological sciences.

MLA

Naseer Muhammad Imran, Rasool Mahmood, Jan Mohammed M, Chaudhary Adeel G, Pushparaj Peter Natesan, Abuzenadah Adel M and Al-Qahtani Mohammad H. A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family. : Journal of the neurological sciences. 20170526.