Encephalomyopathy and optic atrophy with tall stature and mitochondrial dysfunction: a new syndrome.
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Publisher’s version
Publication year
2007Source
Clinical Dysmorphology, 16, 2, (2007), pp. 131-4ISSN
Publication type
Article / Letter to editor
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Organization
Paediatrics - OUD tm 2017
Human Genetics
Neurology
Journal title
Clinical Dysmorphology
Volume
vol. 16
Issue
iss. 2
Page start
p. 131
Page end
p. 4
Subject
DCN 2: Functional Neurogenomics; IGMD 3: Genomic disorders and inherited multi-system disorders; IGMD 4: Glycostation disorders; IGMD 8: Mitochondrial medicine; IGMD 9: Renal disorder; NCMLS 4: Energy and redox metabolism; NCMLS 6: Genetics and epigenetic pathways of disease; ONCOL 3: Translational research; UMCN 3.1: Neuromuscular development and genetic disorders; UMCN 5.1: Genetic defects of metabolism; UMCN 5.3: Cellular energy metabolismThis item appears in the following Collection(s)
- Academic publications [242594]
- Electronic publications [129556]
- Faculty of Medical Sciences [92290]
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