Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report-Reference-Cited by-同舟云学术

Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report

Published:2018-12 Issue:1 Volume:19 Page:
ISSN:1471-2369
Container-title:BMC Nephrology
language:en
Short-container-title:BMC Nephrol

Author:

Sugai Keiji,Ueda Hiroyuki^ORCID,Morimoto Keita,Tanaka Mai,Takahashi Daisuke,Nakashima Akio,Kato Junichiro,Takahashi Hiroshi,Yamaguchi Yutaka,Kawamura Tetsuya,Hanaoka Kazushige,Miyazaki Yoichi,Yokoo Takashi

Publisher

Springer Science and Business Media LLC

Subject

Nephrology

Link

http://link.springer.com/content/pdf/10.1186/s12882-018-1152-6.pdf

Reference34 articles.

1. Maassen JA, Janssen GM, t Hart LM. Molecular mechanisms of mitochondrial diabetes (MIDD). Ann Med 2005;37:213–221. doi: https://doi.org/10.1080/07853890510007188.

2. Iwasaki N, Babazono T, Tsuchiya K, Tomonaga O, Suzuki A, Togashi M, et al. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease. J Hum Genet. 2001;46:330–4. https://doi.org/10.1007/s100380170068 .

3. Yamagata K, Tomida C, Umeyama K, Urakami K, Ishizu T, Hirayama K, et al. Prevalence of Japanese dialysis patients with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene. Nephrol Dial Transplant. 2000;15:385–8. https://doi.org/10.1093/ndt/15.3.385 .

4. Gharavi AG, Kiryluk K, Choi M, Li Y, Hou P, Xie J, et al. Genome-wide association study identifies susceptibility loci for IgA nephropathy. Nat Genet. 2011;43:321–7. https://doi.org/10.1038/ng.787 .

5. Yu XQ, Li M, Zhang H, Low HQ, Wei X, Wang JQ, et al. A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. Nat Genet. 2011;44:178–82. https://doi.org/10.1038/ng.1047 .

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