Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2007-5-15
pubmed:abstractText
To study the frequency and distribution of mutations in SPG3A in a large cohort of patients with hereditary spastic paraplegia.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0003-9942
pubmed:author
pubmed:issnType
Print
pubmed:volume
64
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
706-13
pubmed:meshHeading
pubmed-meshheading:17502470-Adolescent, pubmed-meshheading:17502470-Adult, pubmed-meshheading:17502470-Age of Onset, pubmed-meshheading:17502470-Aged, pubmed-meshheading:17502470-Amides, pubmed-meshheading:17502470-Butyric Acids, pubmed-meshheading:17502470-Child, pubmed-meshheading:17502470-Cohort Studies, pubmed-meshheading:17502470-DNA Mutational Analysis, pubmed-meshheading:17502470-Family Health, pubmed-meshheading:17502470-Female, pubmed-meshheading:17502470-Genetic Predisposition to Disease, pubmed-meshheading:17502470-Humans, pubmed-meshheading:17502470-Male, pubmed-meshheading:17502470-Membrane Proteins, pubmed-meshheading:17502470-Middle Aged, pubmed-meshheading:17502470-Mutation, pubmed-meshheading:17502470-Polyneuropathies, pubmed-meshheading:17502470-Spastic Paraplegia, Hereditary, pubmed-meshheading:17502470-Vesicular Transport Proteins
pubmed:year
2007
pubmed:articleTitle
Hereditary spastic paraplegia 3A associated with axonal neuropathy.
pubmed:affiliation
Laboratory of Molecular Pathology, Sofia Medical University, Sofia, Bulgaria.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't