AKU eCommons
Ehtisham Ul, Haq Makhdoom, S. S. Waseem et al.
· 0 citations
3 papers indexed here
We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.
Not the right person? Other researchers publish under this name.
Open access
Sep 2026
Genetic basis of Charcot-Marie-Tooth disease in Pakistani consanguineous families
Charcot-Marie-Tooth (CMT) is a group of inherited neuromuscular disorders with diverse clinical features such as muscle weakness and atrophy of the distal regions, foot deformities, sensory loss and decreased or absent reflexes. With the diverse inheritance patterns including dominant, recessive, and X-linked, it exhib...
Zafar Ali, M. Jameel, J. Klar et al.
· Frontiers in Neurology · 0 citations
Open access
Sep 2026
Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses.
BACKGROUND Hearing impairment is a genetically heterogeneous disorder and represents a significant health concern, particularly in consanguineous populations where autosomal recessive forms are more prevalent. Pakistani families provide an important population for investigating the genetic basis of hereditary hearing i...
Zafar Ali, Najeeb Ullah, Muneeba Bibi et al.
· Annals of Human Genetics · 0 citations