Exome sequencing identifies a novel homozygous CLN8...

Acta Neurologica Belgica 2017 / 3 Vol. 117; Iss. 1

Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy

Sahin, Yavuz, Güngör, Olcay, Gormez, Zeliha, Demirci, Huseyin, Ergüner, Bekir, Güngör, Gülay, Dilber, Cengiz
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Volume:
117
Language:
english
Journal:
Acta Neurologica Belgica
DOI:
10.1007/s13760-016-0721-3
Date:
March, 2017
File:
PDF, 2.84 MB
english, 2017
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