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Burmese Hypokalemia (BHK) is a disorder associated with a mutation in the WNK4 gene, causing a subnormal serum potassium ion concentration and related clinical symptoms.
10 Arbeidsdager
Spesifikasjoner
| Breeds | |
|---|---|
| Gene | |
| Organ | |
| specimen | Svaber, EDTA blod, heparinblod, sæd, vev |
| Mode of Inheritance | |
| Chromosome | |
| Also known as | |
| Year Published |
Generell informasjon
Burmese Hypokalemia (BHK) is a disorder associated with a mutation in the WNK4 gene, causing a subnormal serum potassium ion concentration and related clinical symptoms. The disorder is recessive and also known as Burmese hypokalaemic periodic polymyopathy (BHP) or Feline Hypokalaemic Periodic Paralysis.
Kliniske egenskaper
Symptomer for affiserte katter er generalisert eller noen ganger lokalisert skjelettmuskulatursvakhet, ofte episodisk i naturen.
Tilleggsinformasjon
Referanser
Pubmed ID: 23285264
Omia ID: 1759