Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta Kristofer Andersson, Barbro Malmgren, Eva Åström, Ann Nordgren, Fulya Taylan and Göran Dahllöf Orphanet Journal of Rare Diseases 2020, 15:80 | Published on: 31 March 2020 Full Text | PDF

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