05.02.18 13:28

CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

Scholl et al., Nat Genet. [in press]

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 Feb 5. doi: 10.1038/s41588-018-0048-5. [Epub ahead of print] PubMed ID: 29403011

 

Further Information:

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undefinedChristoph Fahlke

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