Source:http://linkedlifedata.com/resource/pubmed/id/19446900
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2009-12-7
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pubmed:abstractText |
We describe 7 transplanted heart recipients from a single family with limb-girdle muscular dystrophy type 1B linked to a mutation of the LMNA gene in the splice donor site of the exon 9 (IVS 9+1:g>a). These patients did not display higher early postoperative or late complications than other heart transplant recipients at a mean follow-up of 8 years (range 1-17 years). Noticeably, there was no case of rhabdomyolysis and skeletal muscle symptoms were not markedly impaired.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1874-1754
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
12
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pubmed:volume |
137
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
e75-6
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pubmed:meshHeading |
pubmed-meshheading:19446900-Cardiomyopathy, Dilated,
pubmed-meshheading:19446900-Female,
pubmed-meshheading:19446900-Heart Transplantation,
pubmed-meshheading:19446900-Humans,
pubmed-meshheading:19446900-Lamin Type A,
pubmed-meshheading:19446900-Male,
pubmed-meshheading:19446900-Middle Aged,
pubmed-meshheading:19446900-Muscular Dystrophies, Limb-Girdle,
pubmed-meshheading:19446900-Mutation,
pubmed-meshheading:19446900-Pedigree
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pubmed:year |
2009
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pubmed:articleTitle |
Heart transplantation in 7 patients from a single family with limb-girdle muscular dystrophy caused by lamin A/C mutation.
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pubmed:publicationType |
Letter,
Case Reports
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