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Dive into the research topics of 'Phenotypic spectrum in osteogenesis imperfecta due to mutations in TMEM38B: unravelling a complex cellular defect'. Together they form a unique fingerprint.- Sort by
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Emma Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, Wayne A Cabral, Hannah Titherage, Atif Alsaedi, Vrinda Saraff, Julie Vogt, Trevor Cole, Susan Stewart, Nicola Crabtree, Brandi M Sargent, Sonja Gamsjaeger, Eleftherios P. Paschalis, Paul Roschger, Klaus Klaushofer, Nick J. Shaw, Joan C Marini, Wolfgang Högler
Research output: Contribution to journal › Article › peer-review