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P3.4 Spinal muscular atrophy with respiratory distress type 1 (SMARD-1). A clinico-pathological follow-up

✍ Scribed by B. San Millan-Tejado; S. Teijeira; J.M. Fernandez; C. Navarro


Book ID
116795080
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
45 KB
Volume
21
Category
Article
ISSN
0960-8966

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Infantile spinal muscular atrophy with r
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## Abstract Autosomal recessive spinal muscular atrophy with respiratory distress type 1 (SMARD1) is the second anterior horn cell disease in infants in which the genetic defect has been defined. SMARD1 results from mutations in the gene encoding the immunoglobulin μ‐binding protein 2 (__IGHMBP2__)