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2. DYT16 revisited: Exome sequencing identifies PRKRA mutations in a European dystonia family. Issue 12 (20th August 2014)

3. Identification of two compound heterozygous VPS13A large deletions in chorea‐acanthocytosis only by protein and quantitative DNA analysis. Issue 9 (14th February 2020)

6. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls. Issue 1 (22nd October 2013)