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Clinical highlights of a very rare phospolipid remodeling disease due to MBOAT7 gene defect.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ( IF 2.8 ) Pub Date : 2019-09-11 , DOI: 10.1002/ajmg.b.32762 Ali Dursun 1 , Dilek Yalnızoğlu 2 , Rıza K Özgül 3 , Kader Karlı Oğuz 4 , Didem Yücel-Yılmaz 3
中文翻译：
由于MBOAT7基因缺陷而引起的非常罕见的磷脂重塑疾病的临床亮点。
更新日期：2019-11-01
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ( IF 2.8 ) Pub Date : 2019-09-11 , DOI: 10.1002/ajmg.b.32762 Ali Dursun 1 , Dilek Yalnızoğlu 2 , Rıza K Özgül 3 , Kader Karlı Oğuz 4 , Didem Yücel-Yılmaz 3
Affiliation
中文翻译：
由于MBOAT7基因缺陷而引起的非常罕见的磷脂重塑疾病的临床亮点。
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