Literature DB >> 8411994

Linkage analysis of late-infantile neuronal ceroid-lipofuscinosis (CLN2) using markers on chromosome 16p.

R Williams1, H Mitchison, T Mckay, I Järvelä, R M Gardiner.   

Abstract

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Year:  1993        PMID： 8411994     DOI： 10.1007/bf00710279

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  Infantile neuronal ceroid lipofuscinosis (CLN1): linkage disequilibrium in the Finnish population and evidence that variant late infantile form (variant CLN2) represents a nonallelic locus.

Authors:  I Järvelä
Journal:  Genomics       Date:  1991-06       Impact factor: 5.736

2.  A variant of Jansky-Bielschowsky disease.

Authors:  P Santavuori; J Rapola; K Sainio; C Raitta
Journal:  Neuropediatrics       Date:  1982-08       Impact factor: 1.947

Review 3.  Neuronal ceroid-lipofuscinoses in childhood.

Authors:  P Santavuori
Journal:  Brain Dev       Date:  1988       Impact factor: 1.961

4.  Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12.

Authors:  D F Callen; E Baker; S Lane; J Nancarrow; A Thompson; S A Whitmore; D H MacLennan; R Berger; D Cherif; I Järvelä
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025
  4 in total

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