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A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
title
A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
main subject
amyotrophic lateral sclerosis
0 references
amyotrophic lateral sclerosis type 8
1 reference
based on heuristic
inferred from title
author
Agnes Lumi Nishimura
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Ammar Al-Chalabi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Mayana Zatz
series ordinal
3
object named as
Mayana Zatz
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
publication date
27 September 2005
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
published in
Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
volume
118
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
page(s)
499-500
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
issue
3-4
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
exact match
https://scigraph.springernature.com/pub.10.1007/s00439-005-0031-y
0 references
cites work
Autosomal dominant late adult spinal muscular atrophy, type Finkel
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16187141
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Estimating the age of rare disease mutations: the example of Triple-A syndrome.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16187141
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16187141
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16187141
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16187141
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S00439-005-0031-Y
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
PubMed ID
16187141
1 reference
stated in
Europe PubMed Central
PubMed ID
16187141
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
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