HomozygousKCNMA1mutation as a cause of cerebellar atrophy,...

Human Genetics 2016 / 11 Vol. 135; Iss. 11

HomozygousKCNMA1mutation as a cause of cerebellar atrophy, developmental delay and seizures

Tabarki, Brahim, AlMajhad, Nabil, AlHashem, Amal, Shaheen, Ranad, Alkuraya, Fowzan S.
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Volume:
135
Language:
english
Journal:
Human Genetics
DOI:
10.1007/s00439-016-1726-y
Date:
November, 2016
File:
PDF, 616 KB
english, 2016
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