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A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency

✍ Scribed by Raphael J. Morscher; Sarah Catharina Grünert; Céline Bürer; Patricie Burda; Terttu Suormala; Brian Fowler; Matthias R. Baumgartner


Book ID
116989700
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
166 KB
Volume
105
Category
Article
ISSN
1096-7192

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