在马赛克形式的反复发生的ACTA1氨基酸变化会导致较轻的不对称肌肉病变

Vilma-Lotta Lehtokari1, Lydia Sagath1, Mark Davis2

  • 1Folkhälsan Research Center, 00290 Helsinki, Finland; Department of Medical and Clinical Genetics, Medicum, 00014 University of Helsinki, Finland.

PubMed
概括

马赛克ACTA1变种导致较轻的先天性肌肉病变,而de novo变种导致严重的形式. 马赛克主义可能解释了在动因肌肉病患者的不同疾病严重程度和不对称性.

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