Mitochondrial Dna 8993T > G Mutation in a Child With Ornithine Transcarbamylase Deficiency and Leigh Syndrome: An Unexpected Association

AuthID
 P-002-7KY
6
Author(s)
Henriques, M
·
Document Type
Article
Year published
2012
Published
in JOURNAL OF CHILD NEUROLOGY, ISSN: 0883-0738
Volume: 27, Issue: 8, Pages: 1059-1061 (3)
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Wos®
Scopus®
Crossref®4
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 22241703
SCOPUS: 2-s2.0-84864214971
Wos: WOS:000306610100015
Source Identifiers
ISSN: 0883-0738
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