Work

A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome

Year: 2015

Type: article

Source: Nature Genetics

DOI: 10.1038/ng.3313

Authors: Vafa Alakbarzade, Abdul Hameed, Debra Q Y Quek, Barry A Chioza, Emma L Baple, Amaury Cazenave-Gassiot, Long N Nguyen, Markus R Wenk, Arshia Q Ahmad, Ajith Sreekantan-Nair, Michael N Weedon, Phil Rich, Michael A Patton, Thomas T Warner, David L Silver, Andrew H Crosby

Institutions: University of Exeter, UCL Queen Square Institute of Neurology, University College London, Institute of Biomedical and Genetic Engineering, National University of Singapore, Duke-NUS Medical School, Princess Anne Hospital, University of Southampton, Life Sciences Institute, Rehabilitation Hospital of Indiana, Indiana University – Purdue University Indianapolis, St George's Hospital, National Health Service

Language: English

Topic: Barrier Structure and Function Studies

Subfield: Neurology

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1565002540

FWCI: 7.048

Cites: 12

Cited by: 146

Related to: 10