Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
The original version of this article [1] unfortunately included an error to an author’s name. Author Jordi Díaz-Manera was erroneously presented as Jorge Alberto Diaz Manera. The correct author name has been included in the author list of this Correction article.
Main Authors: | Libby Wood, Guillaume Bassez, Corinne Bleyenheuft, Craig Campbell, Louise Cossette, Aura Cecilia Jimenez-Moreno, Yi Dai, Hugh Dawkins, Jordi Díaz-Manera, Celine Dogan, Rasha el Sherif, Barbara Fossati, Caroline Graham, James Hilbert, Kristinia Kastreva, En Kimura, Lawrence Korngut, Anna Kostera-Pruszczyk, Christopher Lindberg, Bjorn Lindvall, Elizabeth Luebbe, Anna Lusakowska, Radim Mazanec, Giovani Meola, Liannna Orlando, Masanori P. Takahashi, Stojan Peric, Jack Puymirat, Vidosava Rakocevic-Stojanovic, Miriam Rodrigues, Richard Roxburgh, Benedikt Schoser, Sonia Segovia, Andriy Shatillo, Simone Thiele, Ivailo Tournev, Baziel van Engelen, Stanislav Vohanka, Hanns Lochmüller |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2019-08-01
|
Series: | Orphanet Journal of Rare Diseases |
Online Access: | http://link.springer.com/article/10.1186/s13023-019-1157-7 |
Similar Items
-
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
by: Libby Wood, et al.
Published: (2018-09-01) -
Фамилен кортикален миоклоничен тремор и епилепсия
by: Kristina Kastreva, et al.
Published: (2020-10-01) -
Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy
by: Anna Lusakowska, et al.
Published: (2021-03-01) -
Автозомно рецесивна наследствена моторна и сетивна невропатия при мутация в SH3TC2 гена
by: Kristina Kastreva, et al.
Published: (2021-10-01) -
Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness
by: Katherine Johnson, et al.
Published: (2017-11-01)