Thirty one families with Alport syndrome including 3 families with associated syndromes were studied. The location of the COL4A5 gene, responsible for the Alport syndrome, was determined by linkage analysis with eight probes of the Xq arm and by a radiation hybrid panel. Concordant data indicated th
A familial case of mitochondrial disease resembling Alport syndrome
β Scribed by Hayahiko Fujii; Yoshihiro Mori; Kou Kayamori; Toru Igari; Eisaku Ito; Takumi Akashi; Yoshihiro Noguchi; Ken Kitamura; Tomokazu Okado; Yoshio Terada; Eiichiro Kanda; Tatemitsu Rai; Shinichi Uchida; Sei Sasaki
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 350 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1342-1751
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