Severe recurrent renal salt wasting in a boy with a mitochondrial oxidative phosphorylation defect
Author:
Publisher
SAGE Publications
Subject
Clinical Biochemistry,General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1258/0004563001900002
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
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3. Unusual Phenotype and Disease Trajectory in Kearns–Sayre Syndrome;Case Reports in Neurological Medicine;2020-02-28
4. Commentary: New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2;Frontiers in Immunology;2019-06-21
5. Leigh Syndrome Caused by the MT-ND5 m.13513G>A Mutation: A Case Presenting with WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia;JIMD Reports;2014
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