A. Rehman

发表

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15

S. Riazuddin, S. Riazuddin, T. Friedman, 2009, Clinical genetics.

Linkage Analysis of Retinitis Pigmentosa in Families of North Waziristan Agency

Dost Muhammad Khan, F. Ullah, Jabbar Khan, 2017 .

Consanguinity and Autosomal Recessive Mental Retardation in South Waziristan Agency

Jabbar Khan, M. Ismail, A. Rehman, 2017 .

A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy

Z. Kutalik, Y. Kamatani, T. Nakazawa, 2018, Nature Communications.

New variants and in silico analyses in GRK1 associated Oguchi disease

Rachel L. Taylor, C. Rivolta, D. Donnelly, 2020, Human mutation.

A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy

Z. Kutalik, Y. Kamatani, T. Nakazawa, 2018, bioRxiv.

New pathogenic variants and insights into pathogenic mechanisms in GRK1-related Oguchi disease

Rachel L. Taylor, C. Rivolta, D. Donnelly, 2020, bioRxiv.

A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family

Inam Ullah, K. Shah, A. Rehman, 2023, BMC Ophthalmology.

COMPARISON OF RADIOGRAPHIC PATTERN OF ODONTOGENIC PATHOLOGIES OF CHILDREN AND ADULT PATIENTS: A RETROSPECTIVE REVIEW OF HOSPITAL RECORD

T. Ahmad, Basheer Rehman, Muslim Khan, 2021 .

A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA Splicing

C. Rivolta, M. Folcher, M. Quinodoz, 2023, Ophthalmic Research.