Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1991-9-6
pubmed:abstractText
Hyperkalemic periodic paralysis (HYPP) is an autosomal dominant muscle disease with electrophysiological abnormalities suggesting a defect in a voltage-gated sodium channel (NaCh) gene. A human NaCh gene was recently shown to cosegregate with the disease allele in a family with HYPP. Using an independent clone, we have demonstrated close genetic linkage between an NaCh gene and the HYPP locus in another family. With physiological data demonstrating abnormal NaCh function in HYPP patients, the absence of any obligate recombinations in the two families strengthens the argument that this NaCh gene is the site of the defect in this disorder.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-13339316, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-14832379, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-1982991, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2173143, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2434000, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2441469, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2540698, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2549413, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2550145, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2554302, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2558315, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2559760, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2571571, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-2851536, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-3065595, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-3065596, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-3309651, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-3587272, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-3754035, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-3785281, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-3945387, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-4059056, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-5790253, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-6209577, http://linkedlifedata.com/resource/pubmed/commentcorrection/1651050-6329026
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0002-9297
pubmed:author
pubmed:issnType
Print
pubmed:volume
49
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
378-82
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed:year
1991
pubmed:articleTitle
Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.
pubmed:affiliation
Department of Neurology, University of Utah School of Medicine, Salt Lake City 84132.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't