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3. A recessive CLN3 variant is responsible for delayed-onset retinal degeneration in Hereford cattle. Reith RR, Batt MC, Fuller AM, Meekins JM, Diehl KA, Zhou Y, Bedwell PS, Ward JA, Sanders SK, Petersen JL, Steffen DJ. J Vet Diagn Invest; 2024 May; 36(3):438-446. PubMed ID: 38516801 [Abstract] [Full Text] [Related]
4. Neuronal ceroid-lipofuscinosis in a cat. Bildfell R, Matwichuk C, Mitchell S, Ward P. Vet Pathol; 1995 Sep; 32(5):485-8. PubMed ID: 8578638 [Abstract] [Full Text] [Related]
5. Neuronal ceroid lipofuscinosis in Devon cattle is caused by a single base duplication (c.662dupG) in the bovine CLN5 gene. Houweling PJ, Cavanagh JA, Palmer DN, Frugier T, Mitchell NL, Windsor PA, Raadsma HW, Tammen I. Biochim Biophys Acta; 2006 Oct; 1762(10):890-7. PubMed ID: 16935476 [Abstract] [Full Text] [Related]
6. Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog. Hirz M, Drögemüller M, Schänzer A, Jagannathan V, Dietschi E, Goebel HH, Hecht W, Laubner S, Schmidt MJ, Steffen F, Hilbe M, Köhler K, Drögemüller C, Herden C. Mol Genet Metab; 2017 Mar; 120(3):269-277. PubMed ID: 28024876 [Abstract] [Full Text] [Related]
11. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect. de los Reyes E, Dyken PR, Phillips P, Brodsky M, Bates S, Glasier C, Mrak RE. J Child Neurol; 2004 Jan; 19(1):42-6. PubMed ID: 15032383 [Abstract] [Full Text] [Related]
12. Neuronal ceroid lipofuscinosis in a Vietnamese pot-bellied pig (Sus scrofa). Cesta MF, Mozzachio K, Little PB, Olby NJ, Sills RC, Brown TT. Vet Pathol; 2006 Jul; 43(4):556-60. PubMed ID: 16847000 [Abstract] [Full Text] [Related]
13. Clinical and pathologic features of ceroid lipofuscinosis in two Australian cattle dogs. Sisk DB, Levesque DC, Wood PA, Styer EL. J Am Vet Med Assoc; 1990 Aug 01; 197(3):361-4. PubMed ID: 2391273 [Abstract] [Full Text] [Related]
14. Animal model: ceroidosis (ceroid-lipofuscinosis) in Australian cattle dogs. Wood PA, Sisk DB, Styer E, Baker HJ. Am J Med Genet; 1987 Apr 01; 26(4):891-8. PubMed ID: 3591832 [Abstract] [Full Text] [Related]