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Gm1 gangliosidosis (GFB002)
Gm1 gangliosidosis
Specimen type
EDTA whole blood
Contents
GM1 Gangliosidosis is an inherited lysosomal storage disorder. Clinical signs of GM1 gangliosidosis include vision loss, difficulties in walking, loss of balance, head tremors, lethargy and weight loss.
Koart, Siamese