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Article

Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia.

European journal of human genetics : EJHG - 1 Aug 2000

Lund A, Udd B, Juvonen V, Andersen P M, Cederquist K, Ronnevi L O, Sistonen P, Sörensen S A, Tranebjaerg L, Wallgren-Pettersson C, Savontaus M L

Abstract excerpt

We haplotyped 13 Finnish, 10 Swedish, 12 Danish and 2 Norwegian SBMA (spinal and bulbar muscular atrophy, Kennedy disease) families with a total of 45 patients and 7 carriers for 17 microsatellite markers spanning a 25.2 cM region around the androgen receptor gene on chromosome Xq11-q12 in search of a genetic founder effect. In addition, the haplotypes of 50 Finnish, 20 Danish and 22 Swedish control males were...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Motor Neuron Disease

Share to Receptors, Androgen

Share to Repetitive Sequences, Nucleic Acid

Share to Scandinavian and Nordic Countries

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Source

Identifiers

PMID: 10951525
DOI: 10.1038/sj.ejhg.5200517

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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