A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis

By Stogmann E.  

Neurogenetics, Vol. 10, Iss. 1, 2009-02 ,pp. : 73-77

Springer Publishing Company

Access to resources Recommend Favorite

Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis

By Kousi Maria  

Brain, Vol. 132, Iss. 3, 2009-03 ,pp. : 810-819

Oxford University Press

Access to resources Recommend Favorite

Immune cells perturb axons and impair neuronal survival in a mouse model of infantile neuronal ceroid lipofuscinosis

By Groh Janos  

Brain, Vol. 136, Iss. 4, 2013-04 ,pp. : 1083-1101

Oxford University Press

Access to resources Recommend Favorite

Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis

By Siintola Eija   Partanen Sanna   Haapanen Aleksi   Haltia Matti   Maehlen Jan   Lehesjoki Anna-Elina   Tyynelä Jaana  

Brain, Vol. 129, Iss. 6, 2006-06 ,pp. : 1438-1445

Oxford University Press

Access to resources Recommend Favorite

Retinal Pathology and Function in a Cln3 Knockout Mouse Model of Juvenile Neuronal Ceroid Lipofuscinosis (Batten Disease)

By Seigel G.M.   Lotery A.   Kummer A.   Bernard D.J.   Greene N.D.E.   Turmaine M.   Derksen T.   Nussbaum R.L.   Davidson B.   Wagner J.   Mitchison H.M.  

Molecular and Cellular Neuroscience, Vol. 19, Iss. 4, 2002-04 ,pp. : 515-527

Academic Press

Access to resources Recommend Favorite