Specific Sequences of the Sm and Sm-like (Lsm) Proteins Mediate Their Interaction with the Spinal Muscular Atrophy Disease Gene Product (SMN)
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference61 articles.
1. The Genetic Component in Child Mortality
2. The Gene Frequency of Acute Werdnig-Hoffmann Disease (SMA Type 1). A Total Population Survey in North-East England
3. Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy.
4. A hungarian study on Werdnig-Hoffmann disease.
5. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
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