Wolfram Syndrome in the Japanese Population; Molecular Analysis of WFS1 Gene and Characterization of Clinical Features

BACKGROUND: Wolfram syndrome (WFS) is a recessive neurologic and endocrinologic degenerative disorder, and is also known as DIDMOAD (Diabetes Insipidus, early-onset Diabetes Mellitus, progressive Optic Atrophy and Deafness) syndrome. Most affected individuals carry recessive mutations in the Wolfram...

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Detalles Bibliográficos
Autores principales: Matsunaga, Kimie, Tanabe, Katsuya, Inoue, Hiroshi, Okuya, Shigeru, Ohta, Yasuharu, Akiyama, Masaru, Taguchi, Akihiko, Kora, Yukari, Okayama, Naoko, Yamada, Yuichiro, Wada, Yasuhiko, Amemiya, Shin, Sugihara, Shigetaka, Nakao, Yuzo, Oka, Yoshitomo, Tanizawa, Yukio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161373/
https://www.ncbi.nlm.nih.gov/pubmed/25211237
http://dx.doi.org/10.1371/journal.pone.0106906

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161373/
https://www.ncbi.nlm.nih.gov/pubmed/25211237
http://dx.doi.org/10.1371/journal.pone.0106906

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