Suchergebnisse - "Khan, Jamshid"

PubPharm (2)

1

Unveiling genetics of non-syndromic albinism using whole exome sequencing : A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 families

enthalten in: Gene | 2024

von Zaman, Q. | Khan, J. | Ahmad, M. | +23

2

Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families

enthalten in: The journal of gene medicine | 2023

von Zaman, Q. | Iftikhar, A. | Rehman, G. | +12

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