GM2 gangliosidosis AB variant: first case of late onset and review of the literature.

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GM2 gangliosidosis AB variant: first case of late onset and review of the literature.

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By Michael Foley|2022-12-15T14:55:08+00:00August 4, 2022|Comments Off

About the Author: Michael Foley

National Tay-Sachs & Allied Diseases Association (NTSAD) leads the worldwide fight to treat and cure Tay-Sachs, Canavan, GM1, and Sandhoff diseases by driving research, forging collaboration, and fostering community. Supporting families is the center of everything we do.

The content of this website is intended for informational purposes only and not intended to be a substitute for professional medical advice, diagnosis, or treatment.

The National Tay-Sachs & Allied Diseases Association (NTSAD) leads the worldwide fight to treat and cure Tay-Sachs, Canavan, GM1, and Sandhoff diseases by driving research, forging collaboration, and fostering community. Supporting families is the center of everything we do.

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Get the latest news from NTSAD about our Community, the research that provides hope, and what is happening in the world of rare disease.

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Get the latest news from NTSAD about our Community, the research that provides hope, and what is happening in the world of rare disease.

2001 Beacon Street, Suite 204
Boston, MA 02135
(617) 277-4463
info@ntsad.org

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National Tay-Sachs & Allied Diseases Association
2001 Beacon Street, Suite 204, Boston, MA 02135
(617) 277-4463 | info@ntsad.org

Tax ID
#13-1912877

GM2 gangliosidosis AB variant: first case of late onset and review of the literature.

GM2 gangliosidosis AB variant: first case of late onset and review of the literature.

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About the Author: Michael Foley

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