Identification of mutations in the CACNL
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SillΓ©n, Anna; SΓΈrensen, Troels; Kantola, Ilkka; Friis, Mogens Laue; Gustavson, K
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Article
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1997
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John Wiley and Sons
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English
β 136 KB
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Familial hypokalemic periodic paralysis (hypoPP) is an autosomal dominant disorder characterised by episodic attacks of paralysis of varying severity. Recently, linkage was found to markers in 1q31-32 and to the gene encoding the muscle DHP-sensitive calcium channel β£ 1-subunit (CACNL1A3). Subsequen