A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case report

Overview of attention for article published in Journal of Medical Case Reports, November 2015

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A homozygous AHI1 gene mutation in a consanguineous Moroccan family with Joubert syndrome: a case report https://t.co/JvoVhmtvD3

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