A 22q13.1,SOX1010

William Bertani-Torres1,2, Margaux Serey-Gaut3,4, Judite de Oliveira3

  • 1Université Paris Cité, Paris, France.

概括

这项研究详细介绍了一种罕见的瓦登堡综合征 (WS) 病例,该病例是由染色体22q13.1.1.中的马赛克重复引起的. 这些发现扩大了对SOX10基因重复及其相关发育影响的理解.

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