Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases

Gitelman syndrome is an autosomal recessive inherited salt-losing tubulopathy. It has a prevalence of around 1 in 40,000 people, and heterozygous carriers are estimated at approximately 1%, although the exact prevalence is unknown. We estimated the predicted prevalence of Gitelman syndrome based on...

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Detalles Bibliográficos
Autores principales: Kondo, Atsushi, Nagano, China, Ishiko, Shinya, Omori, Takashi, Aoto, Yuya, Rossanti, Rini, Sakakibara, Nana, Horinouchi, Tomoko, Yamamura, Tomohiko, Nagai, Sadayuki, Okada, Eri, Shima, Yuko, Nakanishi, Koichi, Ninchoji, Takeshi, Kaito, Hiroshi, Takeda, Hiroki, Nagase, Hiroaki, Morisada, Naoya, Iijima, Kazumoto, Nozu, Kandai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352941/
https://www.ncbi.nlm.nih.gov/pubmed/34373523
http://dx.doi.org/10.1038/s41598-021-95521-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352941/
https://www.ncbi.nlm.nih.gov/pubmed/34373523
http://dx.doi.org/10.1038/s41598-021-95521-6

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