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Keywords: Human hypomorphic mutations
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Journal Articles
Sevinç Gücüm, Roman Sakson, Marcus Hoffmann, Valerian Grote, Clara Becker, Kaisa Pakari, Lars Beedgen, Christian Thiel, Erdmann Rapp, Thomas Ruppert, Thomas Thumberger, Joachim Wittbrodt
Journal:
Development
Development (2021) 148 (11): dev199385.
Published: 9 June 2021
... the cell type-specific impact of N-glycosylation to be investigated. CDG Human hypomorphic mutations Disease model Glycosylation Medaka Retinitis pigmentosa Protein glycosylation is a crucial prerequisite for proper protein function during the development and maintenance...
Includes: Supplementary data
