Sabiha Nazli
Hospital Sungai Buloh(MY)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Mitochondrial Function and Pathology, RNA and protein synthesis mechanisms, Vestibular and auditory disorders, Ear Surgery and Otitis Media
Most-Cited Works
- → Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome(2015)113 cited
- → Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness(2005)110 cited
- → Mutation spectrum ofMYO7Aand evaluation of a novel nonsyndromic deafnessDFNB2allele with residual function(2008)105 cited
- → The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3(2007)33 cited
- → A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13‐p12(2005)18 cited
- → Targeted sequencing as a tool for genetic mutations screening for familial hypercholesterolaemia patients in Malaysian population(2018)1 cited