Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Paramyotonia congenita (PC), an autosomal dominant muscle disease, shares some clinical and electrophysiological similarities with another myotonic muscle disorder, hyperkalemic periodic paralysis (HYPP). However, clinical and electrophysiologic differences allow differentiation of the two disorders...

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Bibliografski detalji
Glavni autori: Ptacek, L J, Trimmer, J S, Agnew, W S, Roberts, J W, Petajan, J H, Leppert, M
Format: Artigo
Jezik:Inglês
Izdano: 1991
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683172/
https://ncbi.nlm.nih.gov/pubmed/1654742
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