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Springer Nature5
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✓Human Genetics5
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20211
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S. Muhammad results 5 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: S. Muhammad ×Clear All Filters
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A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomesNARA Subscribed
Human Genetics · 2021 · Vol. 140 · Issue 4 · Springer
Muhammad Ali; Shahid Y. Khan; Tony A. Rodrigues; Tânia Francisco; Xiaodong Jiao; Hang Qi; Firoz Kabir; Bushra Irum; Bushra Rauf; Asma A. Khan; Azra Mehmood; Muhammad Asif Naeem; Muhammad Zaman Assir; Muhammad Hassaan Ali; Mohsin Shahzad; Khaled K. Abu-Amero; Shehla Javed Akram; Javed Akram; Sheikh Riazuddin; Saima Riazuddin; Michael L. Robinson; Myriam Baes; Jorge E. Azevedo; J. Fielding Hejtmancik; S. Amer Riazuddin
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GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimatesNARA Subscribed
Human Genetics · 2019 · Vol. 138 · Issue 10 · Springer
Qing Ouyang; Brian C. Kavanaugh; Lena Joesch-Cohen; Bethany Dubois; Qing Wu; Michael Schmidt; Ozan Baytas; Stephen F. Pastore; Ricardo Harripaul; Sasmita Mishra; Abrar Hussain; Katherine H. Kim; Yolanda F. Holler-Managan; Muhammad Ayub; Asif Mir; John B. Vincent; Judy S. Liu; Eric M. Morrow
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The contribution of parent-to-offspring transmission of telomeres to the heritability of telomere length in humansNARA Subscribed
Human Genetics · 2019 · Vol. 138 · Issue 1 · Springer
Dayana A. Delgado; Chenan Zhang; Kevin Gleason; Kathryn Demanelis; Lin S. Chen; Jianjun Gao; Shantanu Roy; Justin Shinkle; Mekala Sabarinathan; Maria Argos; Lin Tong; Alauddin Ahmed; Tariqul Islam; Muhammad Rakibuz-Zaman; Golam Sarwar; Hasan Shahriar; Mahfuzar Rahman; Muhammad Yunus; Jennifer A. Doherty; Farzana Jasmine; Muhammad G. Kibriya; Habibul Ahsan; Brandon L. Pierce
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Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3NARA Subscribed
Human Genetics · 2007 · Vol. 120 · Issue 6 · Springer
Shahid Y. Khan; Saima Riazuddin; Muhammad Tariq; Saima Anwar; Muhammad I. Shabbir; S. Amer Riazuddin; Shaheen N. Khan; Tayyab Husnain; Zubair M. Ahmed; Thomas B. Friedman; Sheikh Riazuddin
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Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3NARA Subscribed
Human Genetics · 2006 · Vol. 118 · Issue 5 · Springer
Peter John; Ghazanfar Ali; Muhammad S. Chishti; Syed Muhammad S. Naqvi; Suzanne M. Leal; Wasim Ahmad
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