Skip to Main Content
SPRIM
  • Consultoría
    • Strategy & Innovation
    • Research & Clinical Services
    • Regulatory & Scientific Affairs
    • Medical Marketing & Engagment
  • Inspiración
    • Noticias y Blog
    • Estudios de caso
    • Publicaciones
  • Acerca de nosotros
    • Liderazgo
    • Localizaciones
  • Localizaciones

Publications

back to all Publications
Publication

Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination

Springer Nature, July 2018

Tamar Harel & Debra Q. Y. Quek & Bernice H. Wong & Amaury Cazenave-Gassiot & Markus R. Wenk & Hao Fan & Itai Berger & Dorit Shmueli & Avraham Shaag & David L. Silver & Orly Elpeleg & Shimon Edvardson
PubMed: PubMed: 30043326
DOI: 10.1007/s10048-018-0556-6
Neuroscience, Cognition, Blood Brain Barrier, Microcephaly
SPRIM Logo
  • Consultoría
    • Strategy & Innovation
    • Research & Clinical Services
    • Regulatory & Scientific Affairs
    • Medical Marketing & Engagment
  • Inspiración
    • Noticias y Blog
    • Estudios de caso
    • Publicaciones
  • Acerca de nosotros
    • Liderazgo
    • Localizaciones

© 2025 SPRIM. All Rights Reserved

  • Privacy Policy
  • Terms & Conditions

© 2025 SPRIM. All Rights Reserved