Infantile spinal muscular atrophy with r
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Katja Grohmann; Raymonda Varon; Piroschka Stolz; Markus Schuelke; Catrin Janetzk
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Article
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2003
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John Wiley and Sons
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English
β 213 KB
## 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 ΞΌβbinding protein 2 (__IGHMBP2__)