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MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12
Lossos, Alexander
Department of Neurology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
Oldfors, Anders
Department of Pathology, University of Gothenburg, Sahlgrenska Hospital, Gothenburg, Sweden.
Fellig, Yakov
Department of Pathology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
Meiner, Vardiella
Department of Genetics, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
Argov, Zohar
Department of Neurology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
Tajsharghi, Homa
Department of Pathology, University of Gothenburg, Sahlgrenska Hospital, Gothenburg, Sweden.
ORCID iD:
0000-0001-8854-5213
Show others and affiliations
2013 (English)
In:
Brain, ISSN 0006-8950, E-ISSN 1460-2156, Vol. 136, no 7, article id e238
Article in journal, Letter (Refereed) Published
Place, publisher, year, edition, pages
Oxford University Press, 2013. Vol. 136, no 7, article id e238
National Category
Neurology
Research subject
Medical sciences
Identifiers
URN:
urn:nbn:se:his:diva-11952
DOI:
10.1093/brain/aws365
ISI:
000321060200007
PubMedID:
23388406
Scopus ID:
2-s2.0-84879979758
OAI: oai:DiVA.org:his-11952
DiVA, id:
diva2:906936
Available from:
2016-02-25
Created:
2016-02-25
Last updated:
2017-11-30
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