父亲UPD (15) 带有致病突变和小超数环染色体15:一个病例报告
David Lee Curtis1, Nasim Bekheirnia2,3, Lorraine Potocki2,4
1Baylor College of Medicine, Houston, Texas, USA.
Case reports in genetics
|August 5, 2025
概括
单亲分裂症 (UPD) 导致巴特特综合征1型通过揭露一个衰退的SLC12A1变体. 这发生在三发症救援和15号染色体的马赛克父亲UPD中.
科学领域:
- 遗传学 是一个遗传学.
- 基因组印记是指基因组的印记.
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
背景情况:
- 单亲分裂性 (UPD) 是一种不寻常的遗传模式,其中一个人仅从一个父母那里继承了染色体的两个副本.
- 这可能会破坏正常的基因功能,并导致各种表型异常.
- 巴特特综合征1型是一种影响功能的遗传性疾病.
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