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Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family

✍ Scribed by Bing-Zhi Yang; Jason M. Mallory; Diane S. Roe; Michele Brivet; G.D. Strobel; Kerri M. Jones; Jia-Huan Ding; Charles R. Roe


Book ID
115639838
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
163 KB
Volume
73
Category
Article
ISSN
1096-7192

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