Open AccessA CLINICAL CASE OF OSTEOGENESIS IMPERFECT TYPE III, DETERMINED BY COL1A1 (P.GLY845ARG) GENE MUTATION IN A NEWBORN GIRL
Author(s) -
I. V. Lastivka,
V. V. Antsupova,
А. Babintseva,
Oksana Ivanivna Yurkiv,
Ljudmila Brisevac,
I. Malieieva
Publication year - 2022
Publication title -
neonatologìâ, hìrurgìâ ta perinatalʹna medicina
Language(s) - English
Resource type - Journals
eISSN - 2413-4260
pISSN - 2226-1230
DOI - 10.24061/2413-4260.xii.1.43.2022.12
Subject(s) - osteogenesis imperfecta , genetics , osteochondrodysplasia , mutation , biology , medicine , pathology , gene