Carnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality
Barbara Burwinkel, Joachim Kreuder, Susanne Schweitzer, Matthias Vorgerd, Klaus Gempel, Klaus-Dieter Gerbitz, Manfred W. KilimannVolume:
261
Year:
1999
Language:
english
Pages:
488
DOI:
10.1006/bbrc.1999.1060
File:
PDF, 50 KB
english, 1999