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Publication

Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities

Journal Contribution - Journal Article

Journal: European Journal of Medical Genetics

ISSN: 1769-7212

Issue: 4

Volume: 58

Pages: 205 - 10

Publication year:2015

WoS Id: 000353995500002
PubMed Id: 25724587
Institutional Repository URL: https://lirias.kuleuven.be/handle/123456789/487021
VABB Id: c:vabb:405857