A new mutation for Huntington disease following maternal transmission of an intermediate allele

Author(s):
Semaka, A.; Kay, C.; Belfroid, R.D.M.; Bijlsma, E.K.; Losekoot, M.; Langen, I.M. van; Maarle, M.C. van; Oosterloo, M.; Hayden, M.R.; Belzen, M.J. van
Published
2015
Publication type
Article / Letter to editor
Huntington diseaseIntermediate alleleNew mutationMaternal CAG repeat expansionHTT gene
Date issued
2015-01-31
Language
English
Is part of
European Journal of Medical Genetics (2015), Vol. 58, no. 1, p. 28-30
hdl
1887/107446
doi
10.1016/j.ejmg.2014.11.005