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Autor:
Kostiantyn V. Rudenko, Lidiia O. Nevmerzhytska, Olha M. Unitska, Polina A. Danchenko, Nadiia S. Leiko
Publikováno v:
Український журнал серцево-судинної хірургії, Vol 30, Iss 4, Pp 73-80 (2022)
Fabry disease (FD) is an X-linked lysosomal storage disease caused by a mutation in the gene encoding α-galactosidase A and leads to reduced activity or complete absence of this enzyme, which causes the accumulation of globotriaosylceramide (Gb3) an
Externí odkaz:
https://doaj.org/article/06c06706e90e48b3b302a61c91153752
