Linked Life Data

15136674

Source:http://linkedlifedata.com/resource/pubmed/id/15136674

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2004-5-11
pubmed:abstractText
To identify the gene and specific mutation underlying hyaline body myopathy in the family studied.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
11
pubmed:volume
62
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1518-21
pubmed:dateRevised
2005-9-19
pubmed:meshHeading
pubmed-meshheading:15136674-Amino Acid Sequence, pubmed-meshheading:15136674-Chromosome Mapping, pubmed-meshheading:15136674-Family, pubmed-meshheading:15136674-Gene Expression, pubmed-meshheading:15136674-Genotype, pubmed-meshheading:15136674-Haplotypes, pubmed-meshheading:15136674-Humans, pubmed-meshheading:15136674-Inclusion Bodies, pubmed-meshheading:15136674-Lod Score, pubmed-meshheading:15136674-Muscle, Skeletal, pubmed-meshheading:15136674-Muscle Proteins, pubmed-meshheading:15136674-Mutation, pubmed-meshheading:15136674-Mutation, Missense, pubmed-meshheading:15136674-Myosin Heavy Chains, pubmed-meshheading:15136674-Neuromuscular Diseases, pubmed-meshheading:15136674-Pedigree, pubmed-meshheading:15136674-Phenotype, pubmed-meshheading:15136674-Polymorphism, Genetic, pubmed-meshheading:15136674-Sarcolemma
pubmed:year
2004
pubmed:articleTitle
Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.
pubmed:affiliation
Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
pubmed:publicationType
Journal Article