Severe Cases of Osteogenesis Imperfecta Type Viii Due to a Homozygous Mutation in P3H1 (Lepre1) and Review of the Literature

AuthID
 P-018-ADH
2
Author(s)
BALA, KA
Document Type
Article
Year published
2021
Published
in Advances in Clinical and Experimental Medicine, ISSN: 1899-5276
Volume: 30, Issue: 12, Pages: 1233-1238
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ISSN: 1899-5276
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