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8. Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23. Sharp JD; Wheeler RB; Lake BD; Savukoski M; Järvelä IE; Peltonen L; Gardiner RM; Williams RE Hum Mol Genet; 1997 Apr; 6(4):591-5. PubMed ID: 9097964 [TBL] [Abstract][Full Text] [Related]
9. Current state of clinical and morphological features in human NCL. Goebel HH; Wisniewski KE Brain Pathol; 2004 Jan; 14(1):61-9. PubMed ID: 14997938 [TBL] [Abstract][Full Text] [Related]
14. [From gene to disease; from CLN1, CLN2 and CLN3 to neuronal ceroid lipofuscinosis]. Taschner PE; Losekoot M; Breuning MH; Hofman I; van Diggelen OP Ned Tijdschr Geneeskd; 2005 Feb; 149(6):300-3. PubMed ID: 15730038 [TBL] [Abstract][Full Text] [Related]
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16. The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses. Weleber RG Eye (Lond); 1998; 12 ( Pt 3b)():580-90. PubMed ID: 9775220 [TBL] [Abstract][Full Text] [Related]
17. Molecular genetics of the neuronal ceroid lipofuscinoses. Mole S; Gardiner M Epilepsia; 1999; 40 Suppl 3():29-32. PubMed ID: 10446748 [TBL] [Abstract][Full Text] [Related]