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
Bildiriler > Özet Bildiri · 2014
Yazarlar: VOLKAN SEYRANTEPE, Seçil AKYILDIZ DEMİR, YIPKIN CALHAN, ZEHRA KEVSER TİMUR, Christian Marsching, Roger Sandhoff, Taeko Miyagi
American Society of Human Genetics 64th Annual Meeting, Amerika Birleşik Devletleri, San Diego, Uluslararası, Poster, Özet Bildiri, 2014-2014, ss 779-779