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List of works by Esmat Fazel-Najafabadi

A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family.

scientific article

Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1.

scientific article

Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset

scientific article published on 27 January 2014

Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran

scientific article published on 2 September 2015

Structural and functional impact of missense mutations in TPMT: An integrated computational approach.

scientific article

Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries

scientific article published on 22 November 2013

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