(Q43263059)

English

Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis

scientific article published on 12 October 2009

Statements

Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis (English)
12 October 2009
278-281

Identifiers

 
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