Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2003-2-4
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D17389, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D45899, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J05200, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M91452, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U50465, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U97329, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X15750, http://linkedlifedata.com/resource/pubmed/xref/OMIM/117000, http://linkedlifedata.com/resource/pubmed/xref/OMIM/145600, http://linkedlifedata.com/resource/pubmed/xref/OMIM/157550, http://linkedlifedata.com/resource/pubmed/xref/OMIM/161800, http://linkedlifedata.com/resource/pubmed/xref/OMIM/180901, http://linkedlifedata.com/resource/pubmed/xref/RefSeq/NM_001036
pubmed:abstractText
The congenital myopathies are a group of disorders characterised by the predominance of specific histological features observed in biopsied muscle. Central core disease and nemaline myopathy are examples of congenital myopathies that have specific histological characteristics but significantly overlapping clinical pictures. Central core disease is an autosomal dominant disorder with variable penetrance which has been linked principally to the gene for the skeletal muscle calcium release channel (RYR1). Two recent reports have identified the 3' transmembrane domain of this gene as a common site for mutations. Two other studies have reported single families that have features of both central core disease and nemaline myopathy (core/rod disease) caused by mutations in RYR1. Screening of the 3' region (exons 93-105) of the RYR1 gene for mutations in 27 apparently unrelated patients with either central core disease or core/rod disease by single strand conformation polymorphism analysis and DNA sequencing identified three described and nine novel mutations in 15 patients.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0960-8966
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
151-7
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:12565913-DNA Mutational Analysis, pubmed-meshheading:12565913-DNA Primers, pubmed-meshheading:12565913-Exons, pubmed-meshheading:12565913-Genes, Dominant, pubmed-meshheading:12565913-Genetic Linkage, pubmed-meshheading:12565913-Genotype, pubmed-meshheading:12565913-Haplotypes, pubmed-meshheading:12565913-Humans, pubmed-meshheading:12565913-Molecular Sequence Data, pubmed-meshheading:12565913-Muscular Diseases, pubmed-meshheading:12565913-Mutation, Missense, pubmed-meshheading:12565913-Myopathy, Central Core, pubmed-meshheading:12565913-Pedigree, pubmed-meshheading:12565913-Peptide Fragments, pubmed-meshheading:12565913-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:12565913-Protein Structure, Tertiary, pubmed-meshheading:12565913-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:12565913-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:12565913-Sequence Homology, Amino Acid
pubmed:year
2003
pubmed:articleTitle
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene.
pubmed:affiliation
Department of Anatomical Pathology, Royal Perth Hospital, Wellington Street,6000, Western Australia, Perth, Australia. mark.davis@health.wa.gov.au
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't