Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Reference9 articles.
1. Muscle Disorders in Childhood;Dubowitz,1995
2. Prenatal onset spinal muscular atrophy;MacLeod;Eur J Paediat Neurol,1999
3. Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region;Korinthenberg;Ann Neurol,1997
4. Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNt gene;Bingham;Neurology,1997
5. Clinical and molecular genetic features of congenital spinal muscular atrophy;Devriendt;Ann Neurol,1996
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