Manninen T

References (3)

Title : Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons - Jalanko_2005_Neurobiol.Dis_18_226
Author(s) : Jalanko A , Vesa J , Manninen T , von Schantz C , Minye H , Fabritius AL , Salonen T , Rapola J , Gentile M , Kopra O , Peltonen L
Ref : Neurobiol Dis , 18 :226 , 2005
Abstract :
PubMedSearch : Jalanko_2005_Neurobiol.Dis_18_226
PubMedID: 15649713
Gene_locus related to this paper: mouse-ppt

Title : Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1 - Jarvela_1991_Genomics_9_170
Author(s) : Jarvela I , Schleutker J , Haataja L , Santavuori P , Puhakka L , Manninen T , Palotie A , Sandkuijl LA , Renlund M , White R , et al.
Ref : Genomics , 9 :170 , 1991
Abstract :
PubMedSearch : Jarvela_1991_Genomics_9_170
PubMedID: 1672288
Gene_locus related to this paper: human-PPT1

Title : Infantile neuronal ceroid-lipofuscinosis is not an allelic form of Batten disease: exclusion of chromosome 16 region with linkage analyses - Jokiaho_1990_Genomics_8_391
Author(s) : Jokiaho I , Puhakka L , Santavuori P , Manninen T , Nyman K , Peltonen L
Ref : Genomics , 8 :391 , 1990
Abstract :
PubMedSearch : Jokiaho_1990_Genomics_8_391
PubMedID: 2249855
Gene_locus related to this paper: human-PPT1