Christoph Kretzschmar
Dresden, SN, Germany
Last Updated: 09/26/2026
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Found 2 publications
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued.
Journal: Orphanet journal of rare diseases
Published: July 04, 2022
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study.
Journal: Orphanet journal of rare diseases
Published: April 08, 2016
Showing 1-2 of 2
Last Updated: 09/26/2026