Published in
Wiley, Human Mutation: Variation, Informatics and Disease, 2(41), p. 420-431, 2019
DOI: 10.1002/humu.23932
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A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotype
Journal article published in 2019 by
Alfonsina Ballester‐Lopez 
,
Emma Koehorst ,
Miriam Almendrote ,
Alicia Martínez‐Piñeiro ,
Giuseppe Lucente ,
Ian Linares‐Pardo ,
Judit Núñez‐Manchón ,
Nicolau Guanyabens ,
Antoni Cano,
Alejandro Lucia ,
Gayle Overend ,
Sarah A. Cumming ,
Darren G. Monckton ,
Teresa Casadevall,
Irina Isern
and other authors.
,
Emma Koehorst ,
Miriam Almendrote ,
Alicia Martínez‐Piñeiro ,
Giuseppe Lucente ,
Ian Linares‐Pardo ,
Judit Núñez‐Manchón ,
Nicolau Guanyabens ,
Antoni Cano,
Alejandro Lucia ,
Gayle Overend ,
Sarah A. Cumming ,
Darren G. Monckton ,
Teresa Casadevall,
Irina Isern
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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