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Characterization of individuals with selected muscular dystrophies from the expanded pilot of the Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet) in the United States
Birth Defects Research ( IF 1.6 ) Pub Date : 2020-07-24 , DOI: 10.1002/bdr2.1764 Bailey Wallace 1, 2 , K Tiffany Smith 2, 3 , Shiny Thomas 4 , Kristin M Conway 5 , Christina Westfield 6 , Jennifer G Andrews 6 , Richard O Weinert 7 , Thuy Quynh N Do 2, 8 , Natalie Street 2 ,
Birth Defects Research ( IF 1.6 ) Pub Date : 2020-07-24 , DOI: 10.1002/bdr2.1764 Bailey Wallace 1, 2 , K Tiffany Smith 2, 3 , Shiny Thomas 4 , Kristin M Conway 5 , Christina Westfield 6 , Jennifer G Andrews 6 , Richard O Weinert 7 , Thuy Quynh N Do 2, 8 , Natalie Street 2 ,
Affiliation
Data on muscular dystrophies (MDs), a heterogeneous group of heritable diseases hallmarked by progressive muscle deterioration, are scarce.
中文翻译：
从美国肌肉萎缩症监测、跟踪和研究网络 (MD STARnet) 扩展试点中对选定肌肉萎缩症患者的特征描述
肌营养不良症 (MDs) 是一组以进行性肌肉退化为特征的异质性遗传疾病，其数据很少。
更新日期：2020-07-24
中文翻译：
从美国肌肉萎缩症监测、跟踪和研究网络 (MD STARnet) 扩展试点中对选定肌肉萎缩症患者的特征描述
肌营养不良症 (MDs) 是一组以进行性肌肉退化为特征的异质性遗传疾病，其数据很少。
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