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6. Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis. Wisniewski KE; Zhong N; Kaczmarski W; Kaczmarski A; Kida E; Brown WT; Schwarz KO; Lazzarini AM; Rubin AJ; Stenroos ES; Johnson WG; Wisniewski TM Ann Neurol; 1998 Jan; 43(1):106-10. PubMed ID: 9450775 [TBL] [Abstract][Full Text] [Related]
7. Protracted course of juvenile ceroid lipofuscinosis associated with a novel CLN3 mutation (p.Y199X). Sarpong A; Schottmann G; Rüther K; Stoltenburg G; Kohlschütter A; Hübner C; Schuelke M Clin Genet; 2009 Jul; 76(1):38-45. PubMed ID: 19489875 [TBL] [Abstract][Full Text] [Related]
8. An autopsy case of adult neuronal ceroid lipofuscinosis. Yazaki M; Totsuka S; Akikusa B; Nagao K Jpn J Psychiatry Neurol; 1986 Dec; 40(4):693-700. PubMed ID: 3599568 [TBL] [Abstract][Full Text] [Related]
9. Progress in neuropathology of the neuronal ceroid lipofuscinoses. Goebel HH; Schochet SS; Jaynes M; Brück W; Kohlschütter A; Hentati F Mol Genet Metab; 1999 Apr; 66(4):367-72. PubMed ID: 10191130 [TBL] [Abstract][Full Text] [Related]
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11. A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy. Licchetta L; Bisulli F; Fietz M; Valentino ML; Morbin M; Mostacci B; Oliver KL; Berkovic SF; Tinuper P Eur J Med Genet; 2015 Oct; 58(10):540-4. PubMed ID: 26360874 [TBL] [Abstract][Full Text] [Related]
12. [Mechanisms of juvenile neuronal ceroid lipofuscinosis (JNCL)]. Wang SY; Jin WN; Wu D Yi Chuan; 2009 Aug; 31(8):779-84. PubMed ID: 19689937 [TBL] [Abstract][Full Text] [Related]
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