Aman Ullah
3PUBLICATIONS
1CO-AUTHORS
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Publications (3)
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|Feb 18, 2026
Integrated genetic and clinical investigation of autosomal dominant hereditary uterine leiomyomas: genotype-phenotype correlation in a pakistani family.Aman Ullah, Nabgha-E -Amen, Sadaf Iftikhar
|Feb 13, 2020
Identification of two novel variants in GAA underlying infantile-onset Pompe disease in two Pakistani families.Aman Ullah, Bibi Zubaida, Huma Arshad Cheema
|Sep 05, 2019
Whole exome sequencing identified a heterozygous KCNJ2 missense variant underlying autosomal dominant familial hypokalemic periodic paralysis in a Pakistani family.Aman Ullah, Ranjha Khan, Muhammad Naeem
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