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Polymerase gamma deficiency (POLG): Clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh’s encephalopathy

✍ Scribed by Emmanuel Scalais; Baudouin Francois; Patrick Schlesser; Rene Stevens; Christian Nuttin; Jean-Jacques Martin; Rudy Van Coster; Sara Seneca; Frank Roels; Gert Van Goethem; Ann Löfgren; Linda De Meirleir


Book ID
119234774
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
592 KB
Volume
16
Category
Article
ISSN
1090-3798

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