(Q24517921)

2 July 2017

title

Rapid diagnostic test for the major mutation underlying Batten disease (English)

1 reference

2 July 2017

0 references

I Järvelä

1

1 reference

2 July 2017

H M Mitchison

2

1 reference

2 July 2017

P B Munroe

3

1 reference

2 July 2017

A M O'Rawe

4

1 reference

2 July 2017

S E Mole

5

1 reference

2 July 2017

A C Syvänen

6

1 reference

2 July 2017

language of work or name

English

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publication date

1 December 1996

1 reference

Journal of Medical Genetics

2 July 2017

published in

1 reference

2 July 2017

volume

33

1 reference

2 July 2017

issue

12

1 reference

2 July 2017

page(s)

1041-1042

1 reference

Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes

2 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050819

Neuronal ceroid-lipofuscinoses in childhood

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050819

Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050819

Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in Finland

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050819

Preferential PCR amplification of alleles: mechanisms and solutions

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050819

Prenatal diagnosis of Batten's disease

30 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9004140

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Isolation of a novel gene underlying Batten disease, CLN3. The International Batten Disease Consortium

1 reference

Crossref

https://api.crossref.org/works/10.1136%2FJMG.33.12.1041

inferred from DOI database lookup

7 January 2021

based on heuristic

Isolation of a novel gene underlying batten disease, CLN3

1 reference

Crossref

https://api.crossref.org/works/10.1136%2FJMG.33.12.1041

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1136/JMG.33.12.1041

1 reference

2 July 2017

0 references

1 reference