Premium
Mutations in ATP1A3 cause alternating hemiplegia of childhood
Author(s) -
Aminkeng F
Publication year - 2013
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12031
Subject(s) - medicine , mutation , pediatrics , genetics , biology , gene
Heterozygous de novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole‐exome sequencing gene‐identification study. Rosewich et al. (2012) Lancet Neurology 11(9):764–773
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom