Muhammad Zaman Khan Assir

Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly

Élodie M. Richard, D.L. Polla, Muhammad Zaman Khan Assir et al. · The American Journal of Human Genetics · 2019 · 92 citations · Full text

Allelic Variant, Developmental Biology, Genetic Disorder +5

Effectiveness of Platelet Transfusion in Dengue Fever: A Randomized Controlled Trial

Muhammad Zaman Khan Assir, Umair Kamran, Hafiz Ijaz Ahmad et al. · Transfusion Medicine and Hemotherapy · 2013 · 85 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

Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development

Ekaterina Ivanova, Frédéric Tran Mau‐Them, Saima Riazuddin et al. · The American Journal of Human Genetics · 2017 · 51 citations · Full text

Developmental Biology, Mendelian Disorder, Brain Development +7

Mutations of <i><scp>SGO2</scp></i> and <i><scp>CLDN14</scp></i> collectively cause coincidental Perrault syndrome

Rabia Faridi, Atteeq U. Rehman, Robert J. Morell et al. · Clinical Genetics · 2016 · 49 citations · Full text

Coincidental Perrault Syndrome, Rare Diseases, Genome Instability +13