Linked Life Data

21623088

Source:http://linkedlifedata.com/resource/pubmed/id/21623088

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-5-30
pubmed:abstractText
Dysferlinopathy is an autosomal recessive-limb girdle muscular dystrophy (AR-LGMD) caused due to the defect in gene encoding dysferlin, a sarcolemmal protein. Awareness of the variants and their relative frequency is essential for accurate diagnosis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0974-5130
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
54
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
350-4
pubmed:meshHeading
pubmed:articleTitle
Dysferlinopathy: spectrum of pathological changes in skeletal muscle tissue.
pubmed:affiliation
Department of Neuropathology, National Institute of Mental Health & Neurosciences, Bangalore, Karnataka, India. gayathrin12@rediffmail.com
pubmed:publicationType
Journal Article