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[Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway]
https://arctichealth.org/en/permalink/ahliterature41604
Source
Tidsskr Nor Laegeforen. 1978 Aug 30;98(24):1145-6
Publication Type
Article
Date
Aug-30-1978
More detail
Author
K H Torp
O. Borud
Source
Tidsskr Nor Laegeforen. 1978 Aug 30;98(24):1145-6
Date
Aug-30-1978
Language
Norwegian
Publication Type
Article
Keywords
Adolescent
Amino Acid Metabolism, Inborn Errors - epidemiology - genetics
Asparagine - urine
Aspartylglucosylaminase - deficiency
Carbohydrate Metabolism, Inborn Errors - epidemiology - genetics
Child
Child, Preschool
English Abstract
Female
Finland - ethnology
Glucosamine - urine
Humans
Infant
Male
Mental Retardation - epidemiology - genetics
Norway
PubMed ID
684720
View in PubMed
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