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Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis
Tae-Hwan Kil, June-Bum KimVolume:
14
Year:
2010
Language:
english
Pages:
4
DOI:
10.1016/j.ejpn.2009.08.004
File:
PDF, 218 KB
english, 2010