Mutation Analysis of the Non-Syndromic Autosomal Recessive Deafness (NSARD) Associated Otoferlin Gene: A Study on Omani Patients Using Bioinformatic Analyses

عناصر مشابهة

• Genomic Studies of Autosomal Recessive Epilepsies in Three Omani Consanguineous Families
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  منشور: (2016)
• Non - Syndromic Autosomal
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  منشور: (2014)
• Mutation Analysis of KIF13B as A Candidate Gene for Autosomal Recessive Hereditary Spastic Paraplegia
  بواسطة: Al-Barwani, Hamida Sarhan
  منشور: (2006)
• Screening for mutations in B-cardiac myosin heavy chain gene among Jordanian patients with familial hypertrophic cardiomyopathy.
  بواسطة: Habbab, Wesal Marwan
  منشور: (2007)
• Screening for 3.7 and 4.2 Deletion Mutations in Sudanese Patients Suspected to Alpha Thalassaemia
  بواسطة: Balloula, Hussam Ali Osman
  منشور: (2017)