| Publication date | Communities | Collections | Article title | Author(s) | Journal/Conference |
|---|---|---|---|---|---|
| 24 Jul 2018 | BMRC | Bioinformatics Institute | Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination | 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 | Neurogenetics |