𝔖 Bobbio Scriptorium
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Screening of the most common mitochondrial DNA mutations among Egyptian pediatric patients with mitochondrial disorders: A one year study

✍ Scribed by Dina Mehaney; Laila Selim; Fayza Hassan


Book ID
119327021
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
57 KB
Volume
12
Category
Article
ISSN
1567-7249

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