Gm1 Gangliosidosis and Sandhoff Disease

Author:

Warner Thomas G.,O’Brien John S.

Publisher

Springer Berlin Heidelberg

Reference104 articles.

1. O’Brien J.S.: The Gangliosidoses. In “The Metabolic Basis of Inherited Disease”, IV Edition. J.B. Stanbury, J.B. Wyngaarden and D.S. Fredrickson (Eds.), New York, McGraw-Hill, Chapter 40, 841–865, 1978.

2. Okada S., O’Brien J.S.: Tay-Sachs disease: generalized absence of a β-D-N-acetylhexosaminidase component. Science 165, 698–700, 1968.

3. Sandhoff K., Harzer K.: Total hexosaminidase deficiency in Tay-Sachs disease (variant O). In “Lysosomes and Storage Diseases”. H.G. Hers and F. Van Hoof (Eds.). New York, Academic Press, 345–356, 1973.

4. Spranger J.W., Langer L.O., Wiedemann H.R.: GM1 gangliosidosis. In “Bone Displasias: an Atlas of Constitutional Disorders of Skeletal Development”. Philadelphia, W.B. Sanders, Co., 171–172, 1974.

5. O’Brien J.S., Bernett J., Veath M.L., Paa D.: Lysosomal storage disorders: diagnosis by ultrastructural examination of skin biopsies. Arch. Neurol. 35, 592–599, 1975.

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