pubmed-article:18297 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18297 | lifeskim:mentions | umls-concept:C0017759 | lld:lifeskim |
pubmed-article:18297 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
pubmed-article:18297 | lifeskim:mentions | umls-concept:C0011155 | lld:lifeskim |
pubmed-article:18297 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:18297 | pubmed:dateCreated | 1977-9-22 | lld:pubmed |
pubmed-article:18297 | pubmed:abstractText | A new case of glucosephosphate isomerase deficiency in a Belgian family is described. The activity of the enzyme was decreased to about 25-30% of the normal value. Characterization of the defect enzyme showed a decreased thermostability. Heating of the enzyme at 45 degrees C showed a loss of activity of 50% after 90 min. The pH-optimum and the KM-value for fructose 6-phosphate were normal. The electrophoretic pattern showed a faster migration. The variant described here differs from all known variants. Therefore we propose to give to this new variant the name GPI-Kortrijk. | lld:pubmed |
pubmed-article:18297 | pubmed:language | eng | lld:pubmed |
pubmed-article:18297 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18297 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18297 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18297 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18297 | pubmed:month | Jul | lld:pubmed |
pubmed-article:18297 | pubmed:issn | 0009-8981 | lld:pubmed |
pubmed-article:18297 | pubmed:author | pubmed-author:StaalG EGE | lld:pubmed |
pubmed-article:18297 | pubmed:author | pubmed-author:EggermontEE | lld:pubmed |
pubmed-article:18297 | pubmed:author | pubmed-author:AkkermanJ WJW | lld:pubmed |
pubmed-article:18297 | pubmed:author | pubmed-author:van... | lld:pubmed |
pubmed-article:18297 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18297 | pubmed:day | 1 | lld:pubmed |
pubmed-article:18297 | pubmed:volume | 78 | lld:pubmed |
pubmed-article:18297 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18297 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18297 | pubmed:pagination | 121-7 | lld:pubmed |
pubmed-article:18297 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
pubmed-article:18297 | pubmed:meshHeading | pubmed-meshheading:18297-Hu... | lld:pubmed |
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pubmed-article:18297 | pubmed:meshHeading | pubmed-meshheading:18297-El... | lld:pubmed |
pubmed-article:18297 | pubmed:meshHeading | pubmed-meshheading:18297-Bl... | lld:pubmed |
pubmed-article:18297 | pubmed:meshHeading | pubmed-meshheading:18297-An... | lld:pubmed |
pubmed-article:18297 | pubmed:meshHeading | pubmed-meshheading:18297-Gl... | lld:pubmed |
pubmed-article:18297 | pubmed:meshHeading | pubmed-meshheading:18297-Ge... | lld:pubmed |
pubmed-article:18297 | pubmed:year | 1977 | lld:pubmed |
pubmed-article:18297 | pubmed:articleTitle | A new variant of glucosephosphate isomerase deficiency: GPI-Kortrijk. | lld:pubmed |
pubmed-article:18297 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18297 | pubmed:publicationType | Case Reports | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18297 | lld:pubmed |