Muhammad Asif Naeem

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh et al. · The American Journal of Human Genetics · 2013 · 238 citations · Full text

Mitochondrial Function, Genetic Disorder, Medicine +7

<i>GNAT1</i>Associated with Autosomal Recessive Congenital Stationary Night Blindness

Muhammad Asif Naeem, Venkata Ramana Murthy Chavali, Shahbaz Ali et al. · Investigative Ophthalmology & Visual Science · 2011 · 73 citations · Full text

<b>Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening</b>

Jianjun Chen, Qiwei Wang, Patricia E. Cabrera et al. · Investigative Ophthalmology & Visual Science · 2017 · 56 citations · Full text

Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families

Lin Li, Yabin Chen, Xiaodong Jiao et al. · Investigative Ophthalmology & Visual Science · 2017 · 48 citations · Full text

Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa

Lin Li, Xiaodong Jiao, Ilaria D’Atri et al. · PLoS Genetics · 2018 · 42 citations · Full text

Ocular Disease, Molecular Physiology, Signal Transduction +13