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Analysis of heavy neurofilament subunit gene polymorphism in Russian patients with sporadic motor neuron disease (MND)

✍ Scribed by Skvortsova, Veronika; Shadrina, Marya; Slominsky, Petr; Levitsky, Gleb; Kondratieva, Ekaterina; Zherebtsova, Anna; Levitskaya, Nina; Alekhin, Alexander; Serdyuk, Anna; Limborska, Svetlana

Book ID: 110025552
Publisher: Nature Publishing Group
Year: 2004
Tongue: English
Weight: 77 KB
Volume: 12
Category: Article
ISSN: 1018-4813
DOI: 10.1038/sj.ejhg.5201144

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## Abstract ## Background: Deletions and duplications of single exons or exon groups account for a large proportion of the __PARK2__ gene mutations described in juvenile autosomal recessive Parkinson's disease (PD). ## Methods: We analyzed rearrangements in exons 1 to 12 of the __PARK2__ gene in