Qaiser Zaman

4PUBLICATIONS
23CO-AUTHORS
Gene mappingElectroanalytical chemistryGene and molecular therapyHaematology
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Publications (4)

|May 08, 2026
The genetic spectrum of achromatopsia in consanguineous families: insights from Whole exome sequencing across 15 affected individuals.

|Apr 29, 2023
Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families.

Qaiser Zaman, Aiman Iftikhar, Gauhar Rehman

|Feb 25, 2023
Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases.

Qaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar

|Jan 21, 2023
Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes.

Qaiser Zaman, Sadeeda, Muhammad Anas

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Frequent Collaborators

4 joint publications

Musharraf Jelani

3 joint publications

Gauhar Rehman

2 joint publications

Ilyas Ahmad

2 joint publications

Osama Yousef Muthaffar