Spinal muscular atrophy: Clinical spectrum and genetic mutations in Pakistani children
Author:
Publisher
Medknow
Subject
Neurology (clinical),Neurology
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Studying carrier frequency of spinal muscular atrophy in the State of Qatar and comparison to other ethnic groups: Pilot study;Molecular Genetics & Genomic Medicine;2023-11-15
2. Experience in prenatal genetic testing and reproductive decision-making for monogenic disorders from a single tertiary care genetics clinic in a low-middle income country;BMC Pregnancy and Childbirth;2023-06-10
3. Gene therapy for selected neuromuscular and trinucleotide repeat disorders – An insight to subsume South Asia for multicenter clinical trials;IBRO Neuroscience Reports;2023-06
4. Spinal muscular atrophy carrier frequency in Saudi Arabia;Molecular Genetics & Genomic Medicine;2022-09-05
5. Carrier frequency of SMN1 ‐related spinal muscular atrophy in north Indian population: The need for population based screening program;American Journal of Medical Genetics Part A;2020-10-14
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