A. Rehman

DFNB86, a novel autosomal recessive non‐syndromic deafness locus on chromosome 16p13.3

S. Riazuddin, S. Riazuddin, Rahima Ali, 2012, Clinical genetics.

Unresolved questions regarding human hereditary deafness.

T. Friedman, A. Rehman, A. Griffith, 2017, Oral diseases.

Genetic causes of moderate to severe hearing loss point to modifiers

T. Friedman, C. Brewer, G. Mujtaba, 2017, Clinical genetics.

INTELLECTUAL DISABILITY CLASSIFICATION, CAUSES, EPIGENETIC MECHANISMS AND TREATMENT

M. Niaz, A. Rehman, S. Anjum, 2023, Biological and Clinical Sciences Research Journal.

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome

W. Newman, Shaheen N. Khan, S. Riazuddin, 2017, Clinical genetics.