Novel heterozygous missense mutation of <i>SLC12A3</i> gene in Gitelman syndrome: A case report. | World J Clin Cases;7(12): 1522-1528, 2019 Jun 26. | MEDLINE

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Novel heterozygous missense mutation of SLC12A3 gene in Gitelman syndrome: A case report.

Wang, Cheng-Lin.

Affiliation

Wang CL; Department of Endocrinology, Shanxi Provincial People's Hospital Affiliated to Shanxi Medical University, Taiyuan 030012, Shanxi Province, China. w15834147610@sina.com.

World J Clin Cases ; 7(12): 1522-1528, 2019 Jun 26.

Article in En | MEDLINE | ID: mdl-31363482

Key words

Bioinformatics analysis; Case report; Gitelman syndrome; High-throughput sequencing; SLC12A3

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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: World J Clin Cases Year: 2019 Document type: Article Affiliation country: China Country of publication: United States

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: World J Clin Cases Year: 2019 Document type: Article Affiliation country: China Country of publication: United States