Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy
Titel:
Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy
Auteur:
Lindahl, Katarina Åström, Eva Dragomir, Anca Symoens, Sofie Coucke, Paul Larsson, Sune Paschalis, Eleftherios Roschger, Paul Gamsjaeger, Sonja Klaushofer, Klaus Fratzl-Zelman, Nadja Kindmark, Andreas