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A commentary on homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome.
Journal of Human Genetics ( IF 2.6 ) Pub Date : 2017-06-16 , DOI: 10.1038/jhg.2017.64 Josef Finsterer 1 , Sinda Zarrouk-Mahjoub 2
中文翻译:
对ISCA1中纯合p。(Glu87Lys)变体的评论与多线粒体功能障碍综合征相关。
更新日期:2019-11-01
Journal of Human Genetics ( IF 2.6 ) Pub Date : 2017-06-16 , DOI: 10.1038/jhg.2017.64 Josef Finsterer 1 , Sinda Zarrouk-Mahjoub 2
Affiliation
中文翻译:
对ISCA1中纯合p。(Glu87Lys)变体的评论与多线粒体功能障碍综合征相关。