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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1981-2-24
|
| pubmed:abstractText |
The case history, laboratory findings and properties of the enzyme in a patient with hexokinase deficiency are reported. The mother had a haemolytic disorder of similar severity. In these cases the expression of the disease in both mother and son suggests a dominant mode of inheritance. This family further illustrates the necessity of taking the reticulocyte level into account when interpreting red cell enzyme levels.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Dec
|
| pubmed:issn |
0007-1048
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
46
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
537-47
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:7437332-Adult,
pubmed-meshheading:7437332-Anemia, Hemolytic, Congenital Nonspherocytic,
pubmed-meshheading:7437332-Erythrocytes,
pubmed-meshheading:7437332-Female,
pubmed-meshheading:7437332-Hexokinase,
pubmed-meshheading:7437332-Humans,
pubmed-meshheading:7437332-Male,
pubmed-meshheading:7437332-Reticulocytes
|
| pubmed:year |
1980
|
| pubmed:articleTitle |
Non-spherocytic haemolytic anaemia in mother and son associated with hexokinase deficiency.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|