23.03.18 17:07

CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

Scholl et al., Nat Genet. 2018

Scholl UI, Stölting G, Schewe J, Thiel A, Tan H, Nelson-Williams C, Vichot AA, Jin SC, Loring E, Untiet V, Yoo T, Choi J, Xu S, Wu A, Kirchner M, Mertins P, Rump LC, Onder AM, Gamble C, McKenney D, Lash RW, Jones DP, Chune G, Gagliardi P, Choi M, Gordon R, Stowasser M, Fahlke C, Lifton RP.

CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

Nat Genet. 2018 Mar;50(3):349-354. doi: 10.1038/s41588-018-0048-5. Epub 2018 Feb 5. PubMed ID: 29403011

 

Further Information:

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undefinedChristoph Fahlke

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