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Seven novel mutations in the ATP2A2 gene of Austrian patients with Darier’s disease

✍ Scribed by A. Klausegger; E. Nischler; R. N. Wagner; F. Pletschacher; H. Hintner; Johann W. Bauer

Publisher
Springer-Verlag
Year
2011
Tongue
English
Weight
402 KB
Volume
303
Category
Article
ISSN
0340-3696

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## Abstract To investigate the frequency of mutations in the Leucine‐Rich Repeat Kinase 2 gene (__LRRK2__) in a sample of Austrian Parkinson's disease (PD) patients, we sequenced the complete coding region in 16 patients with autosomal dominant PD. Furthermore, we sequenced exons 31, 35, and 41 add