Literature DB >> 9151312

Strategy for mutation detection in CLN3: characterisation of two Finnish mutations.

P B Munroe1, A M O'Rawe, H M Mitchison, I E Järvelä, P Santavuori, T J Lerner, P E Taschner, R M Gardiner, S E Mole.   

Abstract

A strategy for detection of mutations in CLN3, the gene for Batten disease or juvenile onset neuronal ceroid lipofuscinosis, has been devised using a technique which detects conformation polymorphisms and direct sequencing of genomic DNA fragments. We define two mutations found uniquely in Finnish patients, one a large deletion (2.8 kb), the other a point mutation affecting the 5'splice donor site of an intron.

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Year:  1997        PMID: 9151312     DOI: 10.1055/s-2007-973657

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  2 in total

Review 1.  Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses.

Authors:  Sara E Mole; Ruth E Williams; Hans H Goebel
Journal:  Neurogenetics       Date:  2005-09-28       Impact factor: 2.660

2.  The fission yeast model for the lysosomal storage disorder Batten disease predicts disease severity caused by mutations in CLN3.

Authors:  Rebecca L Haines; Sandra Codlin; Sara E Mole
Journal:  Dis Model Mech       Date:  2008-12-22       Impact factor: 5.758

  2 in total

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