Facioscapulohumeral Muscular Dystrophy (FSHD)
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-99-0345-0_12
Reference7 articles.
1. Wijmenga C, et al. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4. Lancet. 1990;336(8716):651–3.
2. Lemmers RJ, et al. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2. Nat Genet. 2012;44(12):1370–4.
3. Horwitz MT, Tocantins LM. Isolated paralysis of the serratus anterior (magnus) muscle. J Bone Jt Surg Am. 1938;20(3):720–5.
4. Copeland SA, et al. The shoulder in patients with muscular dystrophy. Clin Orthop Relat Res. 1999;368:80–91.
5. Van Tongel A, et al. Medium to long-term outcome of thoracoscapular arthrodesis with screw fixation for facioscapulohumeral muscular dystrophy. J Bone Jt Surg Am. 2013;95(15):1404–8.
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