E-mail a Wiley Online Library Link

F Aminkeng HINT1 mutations define a novel disease entity – autosomal recessive axonal neuropathy with neuromyotonia Clinical Genetics 83

Article first published online: 29 OCT 2012 | DOI: 10.1111/cge.12030

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

Choose captcha format: Image or Audio. Click here if you need help.