## Abstract We performed sequence analysis of all the exons and exon–intron boundaries in familial and young‐onset Parkinson's disease (PD) in an Asian cohort. None of the patients carried any pathogenic mutations in the Nurr1 gene. We demonstrated a 5 to 10% prevalence of the intron 7 +33 C→T vari
✦ LIBER ✦
Assessment of Nurr1 nucleotide variations in familial Parkinson’s disease
✍ Scribed by C Levecque; A Destée; V Mouroux; P Amouyel; M.-C Chartier-Harlin
- Book ID
- 116766815
- Publisher
- Elsevier Science
- Year
- 2004
- Tongue
- English
- Weight
- 63 KB
- Volume
- 366
- Category
- Article
- ISSN
- 0304-3940
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