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pro vyhledávání: '"Yu. O. Vaseneva"'
Autor:
I. A. Tuzankina, M. A. Bolkov, N. S. Zhuravleva, Yu. O. Vaseneva, Kh. Shinvari, O. V. Schipacheva
Publikováno v:
Медицинская иммунология, Vol 22, Iss 3, Pp 569-576 (2020)
This article presents two clinical cases of patients with a homozygous deletion of segment of chromosome 1, which covers regions of genes associated with complement factor H, in particular CFHR3. Patients underwent in-depth clinical studies, heredity
Externí odkaz:
https://doaj.org/article/979ddc913ffe41a989d3c485bc7ca3b7
