|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1-2
|
|
pubmed:dateCreated |
2010-3-8
|
|
pubmed:abstractText |
Copper deficiency has been described as resulting in severe neurological impairment. However, mechanisms underlying a copper deficiency are presently unknown.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Apr
|
|
pubmed:issn |
1878-5883
|
|
pubmed:author |
|
|
pubmed:copyrightInfo |
Copyright 2010 Elsevier B.V. All rights reserved.
|
|
pubmed:issnType |
Electronic
|
|
pubmed:day |
15
|
|
pubmed:volume |
291
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
95-7
|
|
pubmed:meshHeading |
pubmed-meshheading:20149918-Adult,
pubmed-meshheading:20149918-Ataxia,
pubmed-meshheading:20149918-Cation Transport Proteins,
pubmed-meshheading:20149918-Copper,
pubmed-meshheading:20149918-DNA Mutational Analysis,
pubmed-meshheading:20149918-Deficiency Diseases,
pubmed-meshheading:20149918-Female,
pubmed-meshheading:20149918-Humans,
pubmed-meshheading:20149918-Male,
pubmed-meshheading:20149918-Middle Aged,
pubmed-meshheading:20149918-Muscle Spasticity,
pubmed-meshheading:20149918-Polymorphism, Single Nucleotide,
pubmed-meshheading:20149918-Reflex, Abnormal
|
|
pubmed:year |
2010
|
|
pubmed:articleTitle |
Copper deficiency associated with severe neurological disorder--a genetic work-up of possible mutations in copper transport proteins.
|
|
pubmed:affiliation |
Department of Neurology, Philipps-University Marburg, Rudolf-Bultmann-Strasse 8, 35039 Marburg, Germany.
|
|
pubmed:publicationType |
Journal Article,
Case Reports
|
