Clinical highlights of a very rare phospolipid remodeling disease due to MBOAT7 gene defect

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Bibliographic Details
Published inAmerican journal of medical genetics. Part B, Neuropsychiatric genetics Vol. 183; no. 1; pp. 3 - 4
Main Authors Dursun, Ali, Yalnızoğlu, Dilek, Özgül, Rıza K., Karlı Oğuz, Kader, Yücel‐Yılmaz, Didem
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.01.2020
Wiley Subscription Services, Inc
Subjects
Acyltransferases
Genetic Predisposition to Disease
Genetics
Humans
Intellectual Disability
Membrane Proteins - genetics
Polymorphism, Single Nucleotide
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Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ObjectType-Commentary-2
ISSN:1552-4841
1552-485X
DOI:10.1002/ajmg.b.32762