Faiqa Imtiaz
0000-0002-2961-5733
5 papers found
Refreshing results…
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss
Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia
A retrospective biochemical, molecular, and neurocognitive review of Saudi patients with argininosuccinic aciduria
Twenty novel mutations in BCKDHA , BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden
Missing publications? Search for publications with a matching author name.