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Molecular analysis of HEXA gene in Argentinean patients affected with Tay–Sachs disease: Possible common origin of the prevalent c.459 + 5A>G mutation

✍ Scribed by Stefania Zampieri; Annalisa Montalvo; Mariana Blanco; Irene Zanin; Hernan Amartino; Kristian Vlahovicek; Marina Szlago; Andrea Schenone; Gabriela Pittis; Bruno Bembi; Andrea Dardis


Book ID
116508808
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
173 KB
Volume
499
Category
Article
ISSN
0378-1119

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