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Aldolase B A149P mutation and hereditary fructose intolerance are not associated with sudden infant death syndrome.
https://arctichealth.org/en/permalink/ahliterature59281
Source
Acta Paediatr. 1995 Aug;84(8):947-8
Publication Type
Article
Date
Aug-1995
More detail
Author
N K Aarskog
D. Ogreid
Author Affiliation
Centre of Molecular Medicine, Haukeland Hospital, Bergen, Norway.
Source
Acta Paediatr. 1995 Aug;84(8):947-8
Date
Aug-1995
Language
English
Publication Type
Article
Keywords
Chromosome Aberrations - genetics
Chromosome Disorders
DNA Mutational Analysis
Exons - genetics
Feasibility Studies
Female
Fructose Intolerance - genetics
Fructose-Bisphosphate Aldolase - genetics
Genes, Recessive - genetics
Heterozygote Detection
Homozygote
Humans
Infant
Male
Norway
Point Mutation - genetics
Research Support, Non-U.S. Gov't
PubMed ID
7488826
View in PubMed
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