Focal segmental glomerulosclerosis with a mutation in the mitochondrially encoded NADH dehydrogenase 5 gene: A case report-Reference-Cited by-同舟云学术

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Focal segmental glomerulosclerosis with a mutation in the mitochondrially encoded NADH dehydrogenase 5 gene: A case report

Published:2023-06 Issue: Volume:35 Page:100963
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Naganuma Tsukasa,Imasawa Toshiyuki,Nukui Ikuo,Wakasugi Masakiyo,Kitamura Hiroshi,Yatsuka Yukiko,Kishita Yoshihito,Okazaki Yasushi,Murayama Kei,Jinguji Yoshimi

Funder

Japan Agency for Medical Research and Development

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference52 articles.

1. Minimum birth prevalence of mitochondrial respiratory chain disorders in children;Skladal;Brain.,2003

2. Mitochondrial DNA and disease;Dimauro;Ann. Med.,2005

3. Approaches to finding the molecular basis of mitochondrial oxidative phosphorylation disorders;Kirby;Twin Res. Hum. Genet.,2008

4. Subacute necrotizing encephalomyelopathy in an infant;Leigh;J. Neurol. Neurosurg. Psychiatry,1951

5. MELAS: a nationwide prospective cohort study of 96 patients in Japan;Yatsuga;Biochim. Biophys. Acta,2012

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