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  5. Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
  6. Scopus by Title (Ref)

Zahedan Journal of Research in Medical Sciences

The Official Journal of Zahedan University of Medical Sciences

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Scopus by Title (Ref)


1. Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees

- Nasrniya S. , et al.

2. Identification of a novel frameshift mutation in the tecta gene in an iranian family with autosomal nonsyndromic hearing loss

- Mohammadi-Asl J. , et al.

3. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss

- Mehregan H. , et al.

4. Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature

- Talebi F. , et al.

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