Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene Journal Articles Refereed uri icon

Overview

Published in

  • Clinical Genetics

Time

Date/time value

  • 2012

Identity

Digital Object Identifier (DOI)

  • 10.1111/j.1399-0004.2011.01675.x

Additional Document Info

Parent Title

  • CLINICAL GENETICS

Volume

  • 82

Issue

  • 1

Publisher

  • Munksgaard International Publishers