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Peter Lichtner
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researcher
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Works
4
Genetic diagnosis of Mendelian disorders via RNA sequencing
scientific article published on 12 June 2017
Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder
scientific article published on 27 February 2020
Abstract 12059: Incidental Findings in Cardiomyopathy and Channelopathy Genes Among 5891 Individuals Undergoing Whole-exome Sequencing. What Should be Reported?
scientific article
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
scientific article (publication date: 18 November 2004)
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Instance of
Human
Occupation
Researcher
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