Similar articles

• Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes.

  Williams R, Vesa J, Järvelä I, McKay T, Mitchison H, Hellsten E, Thompson A, Callen D, Sutherland G, Luna-Battadano D, et al. Williams R, et al. Am J Hum Genet. 1993 Oct;53(4):931-5. Am J Hum Genet. 1993. PMID: 8213822 Free PMC article.
• A variant form of late infantile neuronal ceroid lipofuscinosis (CLN5) is not an allelic form of Batten (Spielmeyer-Vogt-Sjögren, CLN3) disease: exclusion of linkage to the CLN3 region of chromosome 16.

  Williams R, Santavuori P, Peltonen L, Gardiner RM, Järvelä I. Williams R, et al. Genomics. 1994 Mar 15;20(2):289-90. doi: 10.1006/geno.1994.1168. Genomics. 1994. PMID: 8020979
• 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. de los Reyes E, et al. J Child Neurol. 2004 Jan;19(1):42-6. doi: 10.1177/08830738040190010703. J Child Neurol. 2004. PMID: 15032383
• Molecular genetic analysis of neuronal ceroid lipofuscinosis.

  Mole SE, Gardiner M. Mole SE, et al. Int J Neurol. 1991-1992;25-26:52-9. Int J Neurol. 1991. PMID: 11980063 Review.
• Neuronal ceroid lipofuscinoses.

  Nita DA, Mole SE, Minassian BA. Nita DA, et al. Epileptic Disord. 2016 Sep 1;18(S2):73-88. doi: 10.1684/epd.2016.0844. Epileptic Disord. 2016. PMID: 27629553 Review.