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Results 1 - 10 of 28 for ".2" Potassium Channel
  1. KCNK9 imprinting syndrome 
    ... Czirjak G. Molecular background of leak K+ currents: two-pore domain potassium channels. Physiol Rev. 2010 Apr;90(2):559-605. doi: 10.1152/physrev.00029.2009. ...
    https://medlineplus.gov/genetics/condition/kcnk9-imprinting-syndrome - Genetics
  2. Benign familial neonatal seizures 
    ... convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels. J Neurosci. 2002 Jan 15;22(2):RC199. doi: 10.1523/JNEUROSCI.22-02-j0003. ... Benign Familial Neonatal Convulsions. Neurosci Lett. 2009 Oct 2;462(1):24-9. doi: ... potassium channel subunits: molecular correlates of the M-channel. Science. ...
    https://medlineplus.gov/.../benign-familial-neonatal-seizures - Genetics
  3. Andersen-Tawil syndrome 
    ... usually unknown. These cases are classified as type 2 (ATS2). Studies suggest that variations in at least one other potassium channel gene may underlie the disorder in some of ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  4. Familial hyperaldosteronism 
    ... Citation on PubMed Stowasser M. Primary aldosteronism and potassium ... Opin Pediatr. 2007 Apr;19(2):192-8. doi: 10.1097/MOP.0b013e32801e217c. Citation ...
    https://medlineplus.gov/.../condition/familial-hyperaldosteronism - Genetics
  5. Palmoplantar keratoderma with deafness 
    ... for making a protein called gap junction beta 2, more commonly known as ... 26 transport potassium ions and certain small molecules.Connexin 26 is ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  6. Bart-Pumphrey syndrome 
    ... for making a protein called gap junction beta 2, more commonly known as ... 26 transport potassium ions and certain small molecules.Connexin 26 is ...
    https://medlineplus.gov/genetics/condition/bart-pumphrey-syndrome - Genetics
  7. Keratitis-ichthyosis-deafness syndrome 
    ... for making a protein called gap junction beta 2, more commonly known as ... 26 transport potassium ions and certain small molecules.Connexin 26 is ...
    https://medlineplus.gov/.../keratitis-ichthyosis-deafness-syndrome - Genetics
  8. Hystrix-like ichthyosis with deafness 
    ... for making a protein called gap junction beta 2, more commonly known as ... 26 transport potassium ions and certain small molecules.Connexin 26 is ...
    https://medlineplus.gov/.../hystrix-like-ichthyosis-with-deafness - Genetics
  9. Vohwinkel syndrome 
    ... for making a protein called gap junction beta 2, more commonly known as ... 26 transport potassium ions and certain small molecules.Connexin 26 is ...
    https://medlineplus.gov/genetics/condition/vohwinkel-syndrome - Genetics
  10. Brugada syndrome 
    ... these other genetic changes account for less than two percent of cases of ... that transport calcium or potassium into or out of heart muscle cells. As ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
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