HPRT-APRT-deficient Mice Are Not a Model for Lesch-Nyhan Syndrome

By Engle Sandra J.   Womer Daniel E.   Davies Philip M.   Boivin Greg   Sahota Amrik   Simmonds H. Anne   Stambrook Peter J.   Tischfield Jay A.  

Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1607-1610

Oxford University Press

Access to resources Recommend Favorite

Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis

By Ceballos-Picot Irene   Mockel Lionel   Potier Marie-Claude   Dauphinot Luce   Shirley Thomas L.   Torero-Ibad Raoul   Fuchs Julia   Jinnah H.A.  

Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2317-2327

Oxford University Press

Access to resources Recommend Favorite

Human neural stem cells: a model system for the study of LeschNyhan disease neurological aspects

By Cristini Silvia   Navone Stefania   Canzi Laura   Acerbi Francesco   Ciusani Emilio   Hladnik Uros   de Gemmis Paola   Alessandri Giulio   Colombo Augusto   Parati Eugenio   Invernici Gloria  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1939-1950

Oxford University Press

Access to resources Recommend Favorite

Lesch-Nyhan Syndrome: Models, Theories, and Therapies

By  

Molecular Syndromology, Vol. 7, Iss. 6, 2016-09 ,pp. : 302-311

Karger

Access to resources Recommend Favorite

Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders

By Nguyen Lam S.   Kim Hyung-Goo   Rosenfeld Jill A.   Shen Yiping   Gusella James F.   Lacassie Yves   Layman Lawrence C.   Shaffer Lisa G.   Gécz Jozef  

Human Molecular Genetics, Vol. 22, Iss. 9, 2013-05 ,pp. : 1816-1825

Oxford University Press

Access to resources Recommend Favorite