Mice with combined deficiencies of β-Hexosaminidase A and Sialidase Neu3 mimic the fundamental aspects of the neurological abnormalities of Tay-Sachs disease due to accumulation of ganglioside: New hope for Tay-Sachs patients and families

Conference paper > Summary Text · 2014

Authors: VOLKAN SEYRANTEPE, Seçil AKYILDIZ DEMİR, YIPKIN CALHAN, ZEHRA KEVSER TİMUR, Christian Marsching, Roger Sandhoff, Taeko Miyagi

American Society of Human Genetics 64th Annual Meeting, United States, San Diego, International, Poster, Summary Text, 2014-2014, pp 779-779

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