S. Basit

发表

Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population

Ameen Softah, Sibtain Afzal, N. Al-Numair, 2019, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families

W. Ahmad, Irfanullah, S. Wakil, 2018, Clinical and experimental dermatology.

Woodhouse–Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene

W. Ahmad, K. Ramzan, K. Shah, 2020, Clinical and experimental dermatology.