Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study

Title
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study
Authors
Keywords
-
Journal
LANCET NEUROLOGY
Volume 11, Issue 9, Pages 764-773
Publisher
Elsevier BV
Online
2012-07-30
DOI
10.1016/s1474-4422(12)70182-5

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