The genetics of spinal muscular atrophies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference75 articles.
1. Identification and characterization of a spinal muscular atrophy-determining gene
2. Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy
3. Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene
4. Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype
5. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
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