Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome.
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| Title: | Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome. |
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| Authors: | Ying Q; Department of Endocrinology and Metabolism, Taizhou Municipal Hospital, Taizhou, Zhejiang, People's Republic of China., Ye Z; Department of Neurology, Taizhou Municipal Hospital, Taizhou, Zhejiang, People's Republic of China., Zhang W; Department of Endocrinology and Metabolism, Taizhou Municipal Hospital, Taizhou, Zhejiang, People's Republic of China., Pan Y; Department of Endocrinology and Metabolism, Taizhou Municipal Hospital, Taizhou, Zhejiang, People's Republic of China., Dai L; Department of Endocrinology and Metabolism, Taizhou Municipal Hospital, Taizhou, Zhejiang, People's Republic of China., Lin K; Department of Endocrinology and Metabolism, Taizhou Municipal Hospital, Taizhou, Zhejiang, People's Republic of China., Feng X; Department of Endocrinology and Metabolism, School of Medicine, Zhejiang University Affiliated Sir Run Shaw Hospital, Hangzhou, Zhejiang, People's Republic of China., Dong X; Department of Endocrinology and Metabolism, School of Medicine, Zhejiang University Affiliated Sir Run Shaw Hospital, Hangzhou, Zhejiang, People's Republic of China., He F; Department of Endocrinology and Metabolism, Taizhou Municipal Hospital, Taizhou, Zhejiang, People's Republic of China. |
| Source: | Clinical endocrinology [Clin Endocrinol (Oxf)] 2023 Nov; Vol. 99 (5), pp. 474-480. Date of Electronic Publication: 2022 Dec 28. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Blackwell Publishing Country of Publication: England NLM ID: 0346653 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2265 (Electronic) Linking ISSN: 03000664 NLM ISO Abbreviation: Clin Endocrinol (Oxf) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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