SMN gene deletion in variant of infantile spinal muscular atrophy
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Identification and characterisation of a spinal muscular atrophy-determining gene;Lefebvre;Cell,1995
2. PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy;Van der Steege;Lancet,1995
3. Diagnostic criteria for neuromuscular disorders;Emery,1994
4. De novo and inherited deletions of the 5q13 region in spinal muscular atrophies;Melki;Science,1994
5. Workshop report: international SMA collaboration;Munsat;Neuromusc Disord,1991
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