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4. A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case report. Chafai-Elalaoui S; Chalon M; Elkhartoufi N; Kriouele Y; Mansouri M; Attié-Bitach T; Sefiani A; Baala L J Med Case Rep; 2015 Nov; 9():254. PubMed ID: 26541515 [TBL] [Abstract][Full Text] [Related]
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