Ehtisham Ul, Haq Makhdoom, S. S. Waseem et al.
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Shafaq Ramzan, Stephanie Tennstedt, M. Tariq et al.
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Open access
Sep 2026
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
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Open access
Sep 2026
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
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