在一个患有PHA1B的伊朗男孩中,SCNN1A基因的新型同卵性突变
Fatemeh Saffari1, Ensiyeh Bahadoran2, Ali Homaei3
1Children Growth Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran.
概括
第1型伪双子症 (PHA1B) 是一种盐浪费障碍,由表皮道 (ENaC) 基因突变引起. 在患有PHA1B的患者中发现了一种新的SCNN1A突变,突出显示了基因型与表型相关性的需要.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 内分泌学 在内分泌学.
背景情况:
- 类型1 (PHA1) 的伪基类型呈现为脏或全身形式,全身类型 (PHA1B) 由上皮通道 (ENaC) 基因的突变引起.
- 已经记录了超过45种PHA1B变异,影响ENAC的α,β和gamma子单元.
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