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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1996-1-31
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pubmed:databankReference | |
pubmed:abstractText |
Muscle glycogenosis caused by phosphorylase kinase (Phk) deficiency may lead to exercise intolerance, weakness and musculatur atrophy. The gene encoding the muscle isoform of the Phk gamma subunit (gamma M) is one of the candidate genes in which mutations responsible for this condition should be sought. Here, we report the cDNA sequence and the predicted primary structure of the human gamma M subunit.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0340-6717
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
96
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
616-8
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8530014-Amino Acid Sequence,
pubmed-meshheading:8530014-Base Sequence,
pubmed-meshheading:8530014-Cloning, Molecular,
pubmed-meshheading:8530014-DNA, Complementary,
pubmed-meshheading:8530014-Humans,
pubmed-meshheading:8530014-Molecular Sequence Data,
pubmed-meshheading:8530014-Muscles,
pubmed-meshheading:8530014-Phosphorylase Kinase
|
pubmed:year |
1995
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pubmed:articleTitle |
Human cDNA encoding the muscle isoform of the phosphorylase kinase gamma subunit (PHKG1).
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pubmed:affiliation |
Institut für Physiologische Chemie, Medizinische Fakultät, Ruhr-Universität Bochum, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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