Biochemical and Biophysical Research Communications
Volume 261, Issue 2, 2 August 1999, Pages 484-487
Regular ArticleCarnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality
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