Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis-Reference-Cited by-同舟云学术

Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

Published:2000-03 Issue:3 Volume:24 Page:251-256
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Kaplan Joshua M.,H Kim Sung,North Kathryn N.,Rennke Helmut,A Correia Lori,Tong Hui-Qi,Mathis Beverly J.,Rodríguez-Pérez José-Carlos,Allen Philip G.,Beggs Alan H.,Pollak Martin R.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0300_251.pdf

Reference28 articles.

1. Ichikawa, I. & Fogo, A. Focal segmental glomerulsoclerosis . Pediatr. Nephrol. 10, 374– 391 (1996).

2. Honda, K. et al. Actinin-4, a novel actin-bundling protein associated with cell motility and cancer invasion. J. Cell. Biol. 140, 1383–1393 (1998); erratum: 143, 276 (1998).

3. Mathis, B.J. et al. A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13: Rapid Communication. Kidney Int. 53, 282–286 (1998).

4. Winn, M. et al. Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity. Genomics 58, 113–120 ( 1999).

5. Fuchshuber, A. et al. Mapping a gene (SRN1) to chromosome 1q25–q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis . Hum. Mol. Genet. 4, 2155– 2158 (1995).

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