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New mutations in the neuronal ceroid lipofuscinosis genes.
Mole, S E; Zhong, N A; Sarpong, A; Logan, W P; Hofmann, S; Yi, W; Franken, P F; van Diggelen, O P; Breuning, M H; Moroziewicz, D; Ju, W; Salonen, T; Holmberg, V; Järvelä, I; Taschner, P E.
Affiliation
  • Mole SE; Department of Paediatrics and Child Health, University College London, Rayne Institute, 5 University Street, London WC1E 6JJ, UK. S.Mole@ucl.ac.uk
Eur J Paediatr Neurol ; 5 Suppl A: 7-10, 2001.
Article in En | MEDLINE | ID: mdl-11589012
ABSTRACT
Thirty-eight mutations and seven polymorphisms have recently been reported in the genes underlying the neuronal ceroid lipofuscinoses (NCLs) including 11 new mutations described here. A total of 114 mutations and 28 polymorphisms have now been described in the five human genes identified which cause NCL. Thirty-eight mutations are recorded for CLN1/PPT; 40 for CLN2/TTP-1, 31 for CLN3, four for CLN5, one for CLN8. Two mutations have been described in animal genes (cln8/mnd, CTSD). All mutations in NCL genes are contained in the NCL Mutation Database (http//www.ucl.ac.uk/NCL).
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Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Neuronal Ceroid-Lipofuscinoses Limits: Child / Humans Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2001 Document type: Article Affiliation country: United kingdom
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Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Neuronal Ceroid-Lipofuscinoses Limits: Child / Humans Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2001 Document type: Article Affiliation country: United kingdom