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10586178
Source:
http://linkedlifedata.com/resource/pubmed/id/10586178
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46
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0011155
,
umls-concept:C0024109
,
umls-concept:C0268436
,
umls-concept:C0332281
,
umls-concept:C0384156
,
umls-concept:C1457887
pubmed:issue
6
pubmed:dateCreated
1999-12-30
pubmed:abstractText
To study patients with autosomal recessive pseudohypoaldosteronism type 1 and to relate pulmonary disease to gene mutations of the epithelial sodium channel (ENaC).
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0375410
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channels
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0022-3476
pubmed:author
pubmed-author:HolmbergLL
,
pubmed-author:KornfältRR
,
pubmed-author:KristofferssonA CAC
,
pubmed-author:MarthinsenLL
,
pubmed-author:NilssonK OKO
,
pubmed-author:OrleniusBB
,
pubmed-author:SchaedelCC
pubmed:issnType
Print
pubmed:volume
135
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
739-45
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10586178-Child, Preschool
,
pubmed-meshheading:10586178-Epithelium
,
pubmed-meshheading:10586178-Female
,
pubmed-meshheading:10586178-Humans
,
pubmed-meshheading:10586178-Lung Diseases
,
pubmed-meshheading:10586178-Mutation
,
pubmed-meshheading:10586178-Polymorphism, Single-Stranded Conformational
,
pubmed-meshheading:10586178-Pseudohypoaldosteronism
,
pubmed-meshheading:10586178-Sequence Analysis, DNA
,
pubmed-meshheading:10586178-Sodium Channels
pubmed:year
1999
pubmed:articleTitle
Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the alpha-subunit of the epithelial sodium channel.
pubmed:affiliation
Department of Pediatrics, University Hospital in Lund, Lund University, Lund, Sweden.
pubmed:publicationType
Journal Article
,
Case Reports
,
Research Support, Non-U.S. Gov't