Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ilya Sergeevich Dantsev"'
Autor:
Alla Nikolaevna Semyachkina, Ekaterina Alexandrovna Nikolaeva, Nailya Mansurovna Galeeva, Alexander Vladimirovich Polyakov, Maria Andreevna Kurnikova, Vera Аlexandrovna Belova, Irina Valerievna Shulyakova, Ilya Sergeevich Dantsev, Goar Vladimirovna Dzhivanshiryan
Publikováno v:
F1000Research, Vol 10 (2021)
Background. This study deals with a rare (orphan) monogenic connective tissue disorder - Ehlers-Danlos syndrome kyphoscoliotic type 2 (EDSKS2). Kyphoscoliotic type 2 Ehlers-Danlos syndrome is an autosomal recessive disorder caused by mutations in the
Externí odkaz:
https://doaj.org/article/5aa8c261f81c4471996d57d0c10d719a
Autor:
A. V. Polyakov, Goar Vladimirovna Dzhivanshiryan, Maria Andreevna Kurnikova, Nailya Mansurovna Galeeva, Irina Valerievna Shulyakova, Ilya Sergeevich Dantsev, A. N. Semyachkina, E.A. Nikolaeva, Vera Belova
Publikováno v:
F1000Research
Background. This study deals with a rare (orphan) monogenic connective tissue disorder - Ehlers-Danlos syndrome kyphoscoliotic type 2 (EDSKS2). Kyphoscoliotic type 2 Ehlers-Danlos syndrome is an autosomal recessive disorder caused by mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fdb4d085c6e21a163695a09b5f9a997
https://doi.org/10.12688/f1000research.52268.1
https://doi.org/10.12688/f1000research.52268.1