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English
Two "new" treatable inherited biosynthetic disorders
scientific article published on 01 August 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
title
Two "new" treatable inherited biosynthetic disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
author name string
J H Walter
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
language of work or name
English
0 references
publication date
1 August 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
volume
348
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
issue
9027
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
page(s)
558-559
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
cites work
Creatine deficiency in the brain: a new, treatable inborn error of metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2964790-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and sequence analysis of human guanidinoacetate N-methyltransferase cDNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2964790-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2964790-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(05)64790-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
PubMed publication ID
8774561
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8774561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8774561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
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