Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism;Ishikawa;Neurology,1996
2. Localisation of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25.2-27;Matsumine;Am J Hum Genet,1997
3. Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region;Jones;Am J Hum Genet,1998
4. Chromosome 6-linked autosomal recessive early-onset parkinsonism: linkage in european and algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family;Tassin;Am J Hum Genet,1998
5. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism;Kitada;Nature,1998
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