回复 格伯等人 的问题. "在遗传性视力缩中的自体递归致病性MSTO1变体"
Anikó Gál1, Janine H Santos2, Mária Judit Molnár1
1Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
EMBO molecular medicine
|July 11, 2023
概括
研究人员证实患者的Misato同类1 (MSTO1) mRNA和蛋白质水平下降. 然而,MSTO1下降的原因尚不清楚,因为确定的突变是在MSTO2p假基因中.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- 之前的研究报告说,患者的Misato同源1 (MSTO1) mRNA和蛋白质水平下降.
- 最近的一项研究发现MSTO2p假基因内的突变.
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