ACTN2 (p.Arg506Gly) 退

Sandra Donkervoort1, Payam Mohassel1, Melanie O'Leary2

  • 1Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.

概括

这项研究在巴勒斯坦患者中发现了一种新的α-actinin-2 (ACTN2) 肌肉疾病的衰退形式,其特征是下肢逐渐疲软. 这些发现扩大了与ACTN2相关的肌肉病变的范围,包括衰退遗传的成人发病情况.

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