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Publications by Eyvind Rødahl
Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome
American Journal of Human Genetics
Genetics
Development of Congenital Stromal Corneal Dystrophy Is Dependent on Export and Extracellular Deposition of Truncated Decorin
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
A Tyrosine Kinase-Activating Variant Asn666Ser in PDGFRB Causes a Progeria-Like Condition in the Severe End of Penttinen Syndrome
European Journal of Human Genetics
Genetics
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Putting Gene Essentiality Into Context
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Bayesian Molecular Clock Dating of Species Divergences in the Genomics Era
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