Mitochondrial DNA mutations in black Americans with hypertension-associated end-stage renal disease-Reference-Cited by-同舟云学术

Mitochondrial DNA mutations in black Americans with hypertension-associated end-stage renal disease

Published:2001-09 Issue:3 Volume:38 Page:529-536
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Watson Bracie,Khan Masood A.,Desmond Renee A.,Bergman Suzanne

Publisher

Elsevier BV

Subject

Nephrology

Reference27 articles.

1. Kidney Involvement in Mitochondrial Disorders;Rotig,1995

2. Congential hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion;Majander;Pediatr Res,1991

3. Deletion of the mitochondrial DNA in a case of DeToni-Debre-Faconi syndrome and Pearson syndrome;Niaudet;Pediatr Nephrol,1994

4. Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia;Rotig;Am J Hum Genet,1992

5. Mitochondrial DNA deletion: A cause of chronic tubulointerstitial nephropathy;Szabolcs;Kidney Int,1994

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