Brecht Guillemyn
0000-0001-7194-6651
Center for Medical Genetics Ghent
2 papers found
Refreshing results…
Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta
Functional characterization of the first missense variant in CEP78 , a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility
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