Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy
Crossref DOI link: https://doi.org/10.1007/s13760-016-0721-3
Published Online: 2016-11-14
Published Print: 2017-03
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Sahin, Yavuz http://orcid.org/0000-0002-7831-067X
Güngör, Olcay
Gormez, Zeliha
Demirci, Huseyin
Ergüner, Bekir
Güngör, Gülay
Dilber, Cengiz
License valid from 2016-11-14