Expanding the phenotype of phospholipid remodelling disease due to MBOAT7 gene defect-Reference-Cited by-同舟云学术

Expanding the phenotype of phospholipid remodelling disease due to MBOAT7 gene defect

Published:2019-01-30 Issue:2 Volume:42 Page:381-388
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Yalnızoǧlu Dilek¹,Özgül R. Köksal²,Oǧuz Kader K.³,Özer Buǧra⁴,Yücel‐Yılmaz Didem²,Gürbüz Berrak⁵,Serdaroǧlu Esra¹,Erol İlknur⁶,Topçu Meral¹,Dursun Ali⁵

Affiliation:

1. Department of Pediatrics, Division of NeurologyHacettepe University Faculty of Medicine Ankara Turkey

2. Hacettepe University Institute of Child Health Ankara Turkey

3. Department of RadiologyHacettepe University Faculty of Medicine Ankara Turkey

4. Advanced Genomics and Bioinformatics Research Center (IGBAM), BILGEMThe Scientific and Technological Research Council of Turkey (TUBITAK) Kocaeli Turkey

5. Department of Pediatrics, Division of MetabolismHacettepe University Faculty of Medicine Ankara Turkey

6. Department of Pediatrics, Division of NeurologyBaskent University Faculty of Medicine Adana Turkey

Funder

Scientific and Technology Research Council of Turkey

Turkey Republic Ministry of Development

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12016

Reference17 articles.