Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Vadim Anatolevich Stepanov"'
Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI
Autor:
Irina Zh. Zhalsanova, Anna Evgenievna Postrigan, Nail Raushanovich Valiakhmetov, Nikita Aleksandrovich Kolesnikov, Daria Ivanovna Zhigalina, Aleksei Andreevich Zarubin, Valeria Viktorovna Petrova, Larisa Ivanovna Minaycheva, Gulnara Narimanovna Seitova, Nikolay Alekseevich Skryabin, Vadim Anatolevich Stepanov
Publikováno v:
International Journal of Molecular Sciences. 24:6672
Osteogenesis imperfecta (OI) is a group of connective tissue disorders with different types of inheritance. OI is characterized by bone fragility and deformities, frequent fractures, low bone-mineral density, and impaired bone micro-architectonics. W
Autor:
Zhalsanova, Irina Zh.1 (AUTHOR) irina.zhalsanova@medgenetics.ru, Postrigan, Anna Evgenievna1 (AUTHOR), Valiakhmetov, Nail Raushanovich1 (AUTHOR), Kolesnikov, Nikita Aleksandrovich1 (AUTHOR), Zhigalina, Daria Ivanovna1 (AUTHOR), Zarubin, Aleksei Andreevich1 (AUTHOR), Petrova, Valeria Viktorovna1 (AUTHOR), Minaycheva, Larisa Ivanovna1 (AUTHOR), Seitova, Gulnara Narimanovna1 (AUTHOR), Skryabin, Nikolay Alekseevich1 (AUTHOR), Stepanov, Vadim Anatolevich1 (AUTHOR) vadim.stepanov@medgenetics.ru
Publikováno v:
International Journal of Molecular Sciences. Apr2023, Vol. 24 Issue 7, p6672. 8p.
Publikováno v:
Genomics & Genetics Weekly; 4/28/2023, p1447-1447, 1p