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pro vyhledávání: '"Matthias Tuerk"'
Autor:
Bjarne Udd, Bruno Eymard, Rosaline Quinlivan, Giorgio Tasca, Taneli Raivio, Lars Edström, Ibrahim Mahjneh, Anni Evilä, Maxwell S. Damian, Fiona Norwood, Frédéric Chevessier, Rolf Schröder, Caroline Sewry, Françoise Chapon, Andoni Echaniz-Laguna, Johanna Palmio, Fengqing Xiang, Jocelyn Laporte, Anders Oldfors, Andrés Berardo, Peter Hackman, Ana Lia Taratuto, Mikko Kärppä, Philipp Gölitz, Matthias Tuerk, Johanna Tommiska, Pascal Laforêt, Jose Antonio Bueri, Carola Hedberg, Björn Brådvik
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry; 85(3), pp 345-353 (2014)
Objective: Several families with characteristic features of hereditary myopathy with early respiratory failure (HMERF) have remained without genetic cause. This international study was initiated to clarify epidemiology and the genetic underlying caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ad8ad10a4331ae3127102355335c445
https://lup.lub.lu.se/record/4417638
https://lup.lub.lu.se/record/4417638
