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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2010-1-7
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pubmed:abstractText |
The authors present the results of a 4-year follow-up of patients with Emery-Dreifuss dystrophy (EDMD) included in a project on laminopathies. The focus of the discussion is on the clinical and genetic characteristics, and the classification of the two forms of Emery-Dreifuss dystrophy [i.e. associated with either emerinopathy (EDMD1) or laminopathy (EDMD2)].
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
0028-3843
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
415-20
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pubmed:meshHeading |
pubmed-meshheading:20054742-DNA,
pubmed-meshheading:20054742-Female,
pubmed-meshheading:20054742-Follow-Up Studies,
pubmed-meshheading:20054742-Heart Diseases,
pubmed-meshheading:20054742-Heterozygote,
pubmed-meshheading:20054742-Humans,
pubmed-meshheading:20054742-Lamin Type A,
pubmed-meshheading:20054742-Male,
pubmed-meshheading:20054742-Membrane Proteins,
pubmed-meshheading:20054742-Muscular Dystrophy, Emery-Dreifuss,
pubmed-meshheading:20054742-Nuclear Proteins,
pubmed-meshheading:20054742-Phenotype
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pubmed:articleTitle |
Emery-Dreifuss dystrophy: a 4-year follow-up on a laminopathy of special interest.
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pubmed:affiliation |
Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw. neurmyol@cmdik.pan.pl
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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