A1 Refereed original research article in a scientific journal
THE GENETIC-LOCUS FOR FREE SIALIC-ACID STORAGE DISEASE MAPS TO THE LONG ARM OF CHROMOSOME-6
Authors: HAATAJA L, SCHLEUTKER J, LAINE AP, RENLUND M, SAVONTAUS ML, DIB C, WEISSENBACH J, PELTONEN L, AULA P
Publisher: UNIV CHICAGO PRESS
Publication year: 1994
Journal: American Journal of Human Genetics
Journal name in source: AMERICAN JOURNAL OF HUMAN GENETICS
Journal acronym: AM J HUM GENET
Volume: 54
Issue: 6
First page : 1042
Last page: 1049
Number of pages: 8
ISSN: 0002-9297
Abstract
Salla disease (SD), or adult-type free sialic acid storage disease, is an autosomal recessive lysosomal storage disorder characterized by impaired transport of free sialic acid across the lysosomal membrane and severe psychomotor retardation. Random linkage analysis of a sample of 27 Finnish families allowed us to localize the SD locus to the long arm of chromosome 6. The highest lod score of 8.95 was obtained with a microsatellite marker of locus D6S286 at theta =.00. Evidence for linkage disequilibrium was observed between the SD locus and the alleles of three closely linked markers, suggesting that the length of the critical region for the SD locus is in the order of 190 kb.
Salla disease (SD), or adult-type free sialic acid storage disease, is an autosomal recessive lysosomal storage disorder characterized by impaired transport of free sialic acid across the lysosomal membrane and severe psychomotor retardation. Random linkage analysis of a sample of 27 Finnish families allowed us to localize the SD locus to the long arm of chromosome 6. The highest lod score of 8.95 was obtained with a microsatellite marker of locus D6S286 at theta =.00. Evidence for linkage disequilibrium was observed between the SD locus and the alleles of three closely linked markers, suggesting that the length of the critical region for the SD locus is in the order of 190 kb.
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