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Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures

Brahim Tabarki; Nabil AlMajhad; Amal AlHashem; Ranad Shaheen; Fowzan S. Alkuraya
Human Genetics · Vol. 135, Issue 11 · pp. 1295-1298 · 2016
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2016-11-01
Publication Year2016
Volume135
Issue11
Pages1295-1298
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-016-1726-y

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
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