Sabiha Nazli

Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome

Mariella Simon, Élodie M. Richard, Xinjian Wang et al. · PLoS Genetics · 2015 · 113 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Mitochondrial Biogenesis +13

Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness

Saima Riazuddin, Shaheen N. Khan, Zubair M. Ahmed et al. · The American Journal of Human Genetics · 2005 · 110 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

Mutation spectrum of<i>MYO7A</i>and evaluation of a novel nonsyndromic deafness<i>DFNB2</i>allele with residual function

Saima Riazuddin, Sabiha Nazli, Zubair M. Ahmed et al. · Human Mutation · 2008 · 105 citations

The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3

Qurat Ul Ain, Sabiha Nazli, Saima Riazuddin et al. · Human Genetics · 2007 · 33 citations

Mendelian Disorder, Genetic Disorder, Genetics +9