Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Katalina Ong"'
Autor:
Katalina Ong, Evan Woodley, Patrick Thompson, Steven J. Gray, Subha Karumuthil-Melethil, Jagdeep S. Walia, Brian L. Mark, Don J. Mahuran, Karlaina J.L. Osmon
Publikováno v:
Molecular Therapy. 23:S283-S284
GM2 gangliosidosis is a group of neurodegenerative disorders, characterized by the malfunctioning Hexosaminidase A (HexA) enzyme, for which there is no treatment. HexA is composed of two similar, but non-identical subunits, the alpha and the beta, wh
Autor:
Karlaina J.L. Osmon, Patrick Thompson, Katalina Ong, Don J. Mahuran, Evan Woodley, Steven J. Gray, Jagdeep S. Walia, Subha Karumuthil-Melethil, Brian L. Mark
Publikováno v:
Journal of Medical Genetics. 52:A4.2-A4
Background G M2 gangliosidosis is a group of neurodegenerative disorders, characterised by the malfunctioning HexosaminidaseA (HexA) enzyme, for which there is no treatment. HexA is composed of two similar, but non-identical subunits, alpha and beta,