The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis

Familial hypokalemic periodic paralysis (HOPP) is a rare autosomal-dominant disease characterized by reversible attacks of muscle weakness occurring with episodic hypokalemia. Mutations in the skeletal muscle calcium (CACNA1S) and sodium channel (SCN4A) genes have been reported to be responsible for...

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Detalles Bibliográficos
Autores principales: Kim, June-Bum, Kim, Man-Ho, Lee, Soon Ju, Kim, Dae-Joong, Lee, Byung Churl
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2007
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694642/
https://www.ncbi.nlm.nih.gov/pubmed/18162704
http://dx.doi.org/10.3346/jkms.2007.22.6.946

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694642/
https://www.ncbi.nlm.nih.gov/pubmed/18162704
http://dx.doi.org/10.3346/jkms.2007.22.6.946

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