APA aipamena

Chafai-Elalaoui, S., Chalon, M., Elkhartoufi, N., Kriouele, Y., Mansouri, M., Attié-Bitach, T., . . . Baala, L. (2015). A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: A case report. J Med Case Rep.

Chicago Style aipamena

Chafai-Elalaoui, Siham, Matthias Chalon, Nadia Elkhartoufi, Yamna Kriouele, Maria Mansouri, Tania Attié-Bitach, Abdelaziz Sefiani, and Lekbir Baala. "A Homozygous AHI1 Gene Mutation (p.Thr304AsnfsX6) in a Consanguineous Moroccan Family With Joubert Syndrome: A Case Report." J Med Case Rep 2015.

MLA aipamena

Chafai-Elalaoui, Siham, et al. "A Homozygous AHI1 Gene Mutation (p.Thr304AsnfsX6) in a Consanguineous Moroccan Family With Joubert Syndrome: A Case Report." J Med Case Rep 2015.