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Exome sequencing as an approach to identify disease causing mutations in pediatric patients with mitochondrial diseases

✍ Scribed by Haack, T.; Strom, T.; Freisinger, P.; Ahting, U.; Rolinski, B.; Mayr, J.; Sperl, W.; Meitinger, T.; Prokisch, H.

Book ID: 122241234
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 57 KB
Volume: 13
Category: Article
ISSN: 1567-7249
DOI: 10.1016/j.mito.2013.07.059

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