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Autor:
Olga N. Ignatovich, Leyla S. Namazova-Baranova, Тea V. Мargieva, Guzal Т. Yakhyaeva, Natalia V. Zhurkova, Кirill V. Savostyanov, Alexander A. Pushkov, Ivan A. Krotov
Publikováno v:
Педиатрическая фармакология, Vol 15, Iss 3, Pp 224-232 (2018)
Osteogenesis imperfect (OI) is a rare genetic disease of connective tissue, the main manifestation are fractures that are developing due to increased bone fragility in both children and adults. Currently, it is known that the genetic basis of the dis
Externí odkaz:
https://doaj.org/article/ad51bd4599e743d7bde725a3f6a8175c
