Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.

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Bibliographic Details
Title: Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.
Authors: Tulinius M; Department of Pediatrics, The Queen Silvia Children's Hospital, Göteborg, Sweden. mar.tulinius@vgregion.se, Moslemi AR, Darin N, Westerberg B, Wiklund LM, Holme E, Oldfors A
Source: Neuropediatrics [Neuropediatrics] 2003 Apr; Vol. 34 (2), pp. 87-91.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Hippokrates Verlag Country of Publication: Germany NLM ID: 8101187 Publication Model: Print Cited Medium: Print ISSN: 0174-304X (Print) Linking ISSN: 0174304X NLM ISO Abbreviation: Neuropediatrics Subsets: MEDLINE
Database: MEDLINE Ultimate
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