✦ LIBER ✦
Carnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality
✍ Scribed by Barbara Burwinkel; Joachim Kreuder; Susanne Schweitzer; Matthias Vorgerd; Klaus Gempel; Klaus-Dieter Gerbitz; Manfred W. Kilimann
- Book ID
- 115584162
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 50 KB
- Volume
- 261
- Category
- Article
- ISSN
- 0006-291X
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