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Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

Document Type

Artikel

Author

Schlingmann, KP; Weber, S; Peters, M; Nejsum, LN; Vitzthum, H; Klingel, K; Kratz, M; Haddad, E; Ristoff, E; Dinour, D; Syrrou, M; Nielsen, S; Sassen, M; Waldegger, S; Seyberth, HW; Konrad, M

Source

Nature genetics. 31(2):166-170

Subject

Medicin och hälsovetenskap

Language

English
English

ISSN

1061-4036

Online Access

EBSCOHost PDF Full Text (Nature Journals) Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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