E-mail a Wiley Online Library Link

Marzia Pasquali and Nicola Longo Response to Chen et al.: Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype–Phenotype Correlation Human Mutation 34

Version of Record online: 20 MAR 2013 | DOI: 10.1002/humu.22285

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field