Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations-Reference-Cited by-同舟云学术

Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations

Published:1999-01 Issue:1 Volume:64 Page:51-61
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lenkkeri Ulla,Männikkö Minna,McCready Paula,Lamerdin Jane,Gribouval Olivier,Niaudet Patrick,Antignac Corinne,Kashtan Clifford E.,Holmberg Christer,Olsen Anne,Kestilä Marjo,Tryggvason Karl

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference30 articles.

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2. Prediction of complete gene structures in human genomic DNA;Burge;J Mol Biol,1997

3. Gene structure, chromosomal location, and basis for alternative mRNA splicing of the human VCAM1 gene;Cybulsky;Proc Natl Acad Sci USA,1991

4. Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population;Fuchshuber;Pediatr Nephrol,1996

5. Nephrotic syndrome in newborn and young infants;Hallman;Ann Paediatr Fenn,1956

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