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Catastrophic Autonomic Crisis With Cardiovascular Collapse in Spinal Muscular Atrophy With Respiratory Distress Type 1

✍ Scribed by Nomura, T.; Takenouchi, T.; Fukushima, H.; Shimozato, S.; Kosaki, K.; Takahashi, T.


Book ID
121450270
Publisher
SAGE Publications
Year
2012
Tongue
English
Weight
200 KB
Volume
28
Category
Article
ISSN
0883-0738

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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__)