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Updated: Mar 17, 2026

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Broad clinical phenotype in Parkinsonism associated with a base pair deletion in RAB39B and additional POLG variant
Max Güldner1, Claudia Schulte1, Ann-Kathrin Hauser1
1University of Tuebingen, Department of Neurodegeneration, Hertie Institute for Clinical Brain Research and German Center of Neurodegenerative Diseases (DZNE), Tuebingen, Germany.
No abstract available in PubMed .
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