Author: "Tawamie, Hasan" / Journal: orphanet journal of rare diseases - Searchworks@Jio Institute Digital Library Search Results

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Start Over Author "Tawamie, Hasan" Journal orphanet journal of rare diseases

1 results on '"Tawamie, Hasan"'

1. SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss

Author: Buchert, Rebecca, primary, Nesbitt, Addie I., additional, Tawamie, Hasan, additional, Krantz, Ian D., additional, Medne, Livija, additional, Helbig, Ingo, additional, Matalon, Dena R., additional, Reis, André, additional, Santani, Avni, additional, Sticht, Heinrich, additional, and Abou Jamra, Rami, additional
Published: 2016
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