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Identification of a Novel Homozygous IHH Variant Causing Novel Acromesomelic Maroteaux-Type Skeletal Dysplasia in a Pakistani Family Cover

Identification of a Novel Homozygous IHH Variant Causing Novel Acromesomelic Maroteaux-Type Skeletal Dysplasia in a Pakistani Family

By: ,  ,  ,  ,  ,  ,   and    
Open Access
|May 2026

Authors

M Hanif

hanifawkum85@gmail.com

Department of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan

B Ahmad

Department of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan

S Farman

sairafarman@awkum.edu.pk

Department of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan

S Hassan

Salmanhassan.ibms@kmu.edu.pk

Department of Biochemistry, institute of Basic Medical Sciences, Khyber Medical University Peshawar, Pakistan

A Hayat

aamir.hayatqau15@gmail.com

Department of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan

N Bibi

drnosheenbibi@sbbwu.edu.pk

Shaheed Benazir Bhutto Women University, Peshawar, Pakistan

U Kalsoom

kalsoom_ibrahim@hotmail.com

Department of Biochemistry, Hazara University, Mansera, Pakistan

B Khan

bushrakhan@awkum.edu.pk

Department of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan
Language: English
Page range: 29 - 40
Published on: May 14, 2026
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2026 M Hanif, B Ahmad, S Farman, S Hassan, A Hayat, N Bibi, U Kalsoom, B Khan, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.