Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel α subunit — a large kindred with a novel phenotype-Reference-Cited by-同舟云学术

Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel α subunit — a large kindred with a novel phenotype

Published:1997-03 Issue:2 Volume:7 Page:105-111
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Kelly P.,Yang W.S.,Costigan D.,Farrell M.A.,Murphy S.,Hardiman O.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference27 articles.

1. Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene;Fontaine;Science,1990

2. Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus;Ptacek;Am J Hum Genet,1991

3. The periodic paralyses and paramyotonia congenita;Lehmann-Horn,1994

4. The skeletal muscle sodium and chloride channel diseases;Hudson;Brain,1995

5. Adynamia episodica hereditaria: what causes the weakness?;Ricker;Muscle Nerve,1989

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