Diagnosis of GM-1 gangliodosis in Cuba
<strong>Background:</strong> GM-1 gangliosidosis is included in the group of lysosomal diseases and is characterized by a deficiency of the enzyme b-galactosidase, which as a consequence produces accumulation of GM1 ganglioside in nervous cells and galactosil oligosaccharides and product...
Saved in:
Main Authors: | Caridad Menéndez Saínz (Author), Sergio González García (Author), Claudina Zaldívar Muñoz (Author), Alina González-Quevedo Monteagudo (Author) |
---|---|
Format: | Book |
Published: |
Centro Provincial de Información de Ciencias Médicas. Cienfuegos,
2007-05-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Diagnosis of GM-1 gangliodosis in Cuba
by: Caridad Menéndez Saínz, et al.
Published: (2007) -
Century of GM
by: Inna B. Bovina
Published: (2024) -
GM1 gangliosidosis: a case report
by: Guilherme Dienstmann, et al.
Published: (2021) -
GM1 Gangliosidosis Type 1 and Mongolian Spots
by: J Gordon Millichap
Published: (2013) -
My Scientific Supervisor - GM: to the 95th Anniversary of G.M. Andreeva
by: Inna B. Bovina
Published: (2019)