𝔖 Bobbio Scriptorium
✦   LIBER   ✦

INa and IKir are reduced in Type 1 hypokalemic and thyrotoxic periodic paralysis

✍ Scribed by Araya Puwanant; Robert L. Ruff


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
416 KB
Volume
42
Category
Article
ISSN
0148-639X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Identification of mutations in the CACNL
✍ SillΓ©n, Anna; SΓΈrensen, Troels; Kantola, Ilkka; Friis, Mogens Laue; Gustavson, K πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 136 KB πŸ‘ 3 views

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 ␣ 1-subunit (CACNL1A3). Subsequen

Acetazolamide opens the muscular K3.0.CO