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Expanding the clinical phenotype of the mitochondrial m.13513G>A mutation with the first report of a fatal neonatal presentation: importance of DNA collection for post-mortem diagnosis

✍ Scribed by ANDREA L. GROPMAN

Book ID: 111131715
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 55 KB
Volume: 53
Category: Article
ISSN: 0012-1622
DOI: 10.1111/j.1469-8749.2011.03920.x

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