Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy
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| Description | scientific article published on 22 June 2018 |
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author: Eleftherios P Paschalis Klaus Klaushofer Sonja Gamsjaeger Nadja Fratzl-Zelman Paul Roschger Andreas Kindmark Anca Dragomir |
| Publication date | June 22, 2018 |
| Language | English |
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