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

AuthID
 P-01B-E4Q
2
Author(s)
Bala, KA
Tipo de Documento
Article
Year published
2021
Publicado
in ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, ISSN: 1899-5276
Volume: 30, Número: 12, Páginas: 1233-1238 (6)
Indexing
Wos®
Scopus®
Pubmed®
Publication Identifiers
Pubmed: 34637196
SCOPUS: 2-s2.0-85117915158
Wos: WOS:000729243000001
Source Identifiers
ISSN: 1899-5276
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