Spinal muscular atrophy – a revisit of the diagnosis and treatment modalities
Author:
Affiliation:
1. Indian Institute of Technology, BHU, Varanasi;
2. School of Biotechnology, BHU, Varanasi
Publisher
Informa UK Limited
Subject
General Medicine,General Neuroscience
Link
https://www.tandfonline.com/doi/pdf/10.1080/00207454.2019.1635128
Reference122 articles.
1. Ueber chronische spinale Muskelatrophie im Kindesalter, auf familiärer Basis
2. Zwei frühinfantile hereditäre Fälle von progressiver Muskelatrophie unter dem Bilde der Dystrophie, aber anf neurotischer Grundlage
3. Newborn and carrier screening for spinal muscular atrophy
4. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
5. Molecular Prenatal Diagnosis of Autosomal Recessive Spinal Muscular Atrophies Using Quantification Polymerase Chain Reaction
Cited by 3 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. NAIP Gene Deletion and SMN2 Copy Number as Molecular Tools in Predicting the Severity of Spinal Muscular Atrophy;Biochemical Genetics;2024-02-22
2. Intelligent Ratio: A New Method for Carrier and Newborn Screening in Spinal Muscular Atrophy;Genetic Testing and Molecular Biomarkers;2020-09-01
3. Correction;International Journal of Neuroscience;2019-12-23
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