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Human Genetics|February 16, 2005
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1Jamil Ahmad, Shaheen N Khan, Shahid Y Khan, et al.
Human Genetics|September 29, 2005
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4Qingjiong Zhang, Fareeha Zulfiqar, Xueshan Xiao, et al.
Scientific Data|September 12, 2018
Whole genome sequencing data for two individuals of Pakistani descentShahid Y Khan, Firoz Kabir, Oussama M'Hamdi, et al.
Clinical Genetics|March 8, 2024
Homozygous novel truncating variant of CLPP associated with severe Perrault syndromeRabia Faridi, Pamela Stratton, Noemi Salmeri, et al.
Heliyon|July 7, 2023
Folicitin abrogates scopolamine induced oxidative stress, hyperlipidemia mediated neuronal synapse and memory dysfunction in miceSeema Gul, Sobia Attaullah, Mahdi H Alsugoor, et al.
Scandinavian Journal of Immunology|March 29, 2025
The Role of Epstein-Barr Virus Molecular Mimicry in Various Autoimmune DiseasesAyesha Munir, Sanaullah Khan, Aisha Saleem, et al.
The British Journal of Ophthalmology|June 12, 2010
Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani familyAmber Shahzadi, S Amer Riazuddin, Shahbaz Ali, et al.
Human Genetics|August 23, 2008
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndromeZubair M Ahmed, Saima Riazuddin, Sandar Aye, et al.
International Journal of Biological Macromolecules|February 9, 2023
Zinc oxide loaded chitosan-elastin-sodium alginate nanocomposite gel using freeze gelation for enhanced adipose stem cell proliferation and antibacterial propertiesAmna Ramzan, Azra Mehmood, Ramla Ashfaq, et al.
Frontiers in Psychology|December 6, 2021
Impact of Role Conflict on Intention to Leave Job With the Moderating Role of Job Embeddedness in Banking Sector EmployeesFazal Hussain Awan, Liu Dunnan, Khalid Jamil, et al.
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