✦ LIBER ✦
Mutation c.106delG (p.Ala36fs*6) associée au syndrome néphrotique congénital type finlandais : premier cas diagnostiqué au Togo
✍ Scribed by Sabi, Kossi Akomola; Noto-Kadou-Kaza, Béfa; Gnionsahe, Dazé Appolinaire; Amekoudi, Eyram Yoan Makafui; Tsevi, Claude Mawufemo; Tsonya, Kokuvi Dzigbodi; Amedegnato, Dégnon; Gnamey, Koffi
- Book ID
- 123303553
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- French
- Weight
- 315 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1769-7255
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