Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures
Crossref DOI link: https://doi.org/10.1007/s00439-016-1726-y
Published Online: 2016-08-27
Published Print: 2016-11
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Tabarki, Brahim
AlMajhad, Nabil
AlHashem, Amal
Shaheen, Ranad
Alkuraya, Fowzan S.
Funding for this research was provided by:
King Abdulaziz City for Science and Technology (by KACST grant 13-BIO1113-20 (FSA).)
License valid from 2016-08-27