Mutation c.106delG (p.Ala36fs*6) associée au syndrome néphrotique congénital type finlandais : premier cas diagnostiqué au Togo-Reference-Cited by-同舟云学术

Mutation c.106delG (p.Ala36fs*6) associée au syndrome néphrotique congénital type finlandais : premier cas diagnostiqué au Togo

Published:2013-12 Issue:7 Volume:9 Page:494-496
ISSN:1769-7255
Container-title:Néphrologie & Thérapeutique
language:fr
Short-container-title:Néphrologie & Thérapeutique

Author:

Sabi Kossi Akomola,Noto-Kadou-Kaza Béfa,Gnionsahe Dazé Appolinaire,Amekoudi Eyram Yoan Makafui,Tsevi Claude Mawufemo,Tsonya Kokuvi Dzigbodi,Amedegnato Dégnon,Gnamey Koffi

Publisher

Elsevier BV

Subject

Nephrology

Reference14 articles.

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2. Congenital nephrotic syndrome of Finnish type. Study of 75 cases;Huttunen;Arch Dis Child,1976

3. Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type;Aya;Kidney Int,2000

4. Congenital nephrotic syndrome of the Finnish type;Badoe;Ghana Med J,2008

5. Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish type;BeomHee;J Korean Med Sci,2009

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