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About this Medicine article
A homozygousAHI1gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case report by Chafai-Elalaoui, Siham; Chalon, Matthias; Elkhartoufi, Nadia; Kriouele, Yamna; Mansouri, Maria; Attié-Bitach, Tania; Sefiani, Abdelaziz; Baala, Lekbir is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Chafai-Elalaoui, Siham; Chalon, Matthias; Elkhartoufi, Nadia; Kriouele, Yamna; Mansouri, Maria; Attié-Bitach, Tania; Sefiani, Abdelaziz; Baala, Lekbir
- Publisher
- BioMed Central; Springer (Biomed Central Ltd.); [London]: BioMed Central, 2007-; [London]: 2008-; Springer Science and Business Media LLC (ISSN 1752-1947)
- Published
- 2015
- Language
- EN
- Field
- Medicine (Health Sciences)