http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23031954

Outgoing Links

Predicate Object
contentType Journal Article
issn 2376-7839
issueIdentifier 6
pageRange e534-
publicationName Neurology. Genetics
startingPage e534
bibliographicCitation Bauché S, Sureau A, Sternberg D, Rendu J, Buon C, Messéant J, Boëx M, Furling D, Fauré J, Latypova X, Gelot AB, Mayer M, Mary P, Whalen S, Fournier E, Cloix I, Remerand G, Laffargue F, Nougues M, Fontaine B, Eymard B, Isapof A, Strochlic L. New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes. Neurol Genet. 2020 Dec;6(6). doi: 10.1212/nxg.0000000000000534.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a13222e512d44bc785f6490f70fc35ea
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e9761823ce522fb11813f59d9e219d9b
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-4449-8683
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d23a1ec43e510b85ac6af4722e7aa00a
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6926-339X
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-1523-0207
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-3660-9809
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4322216e6f4050b5a27e1a47b3e55fcc
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-9156-5047
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-7912-4409
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-5373-4284
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b046f461353bf1aedf24414d82563bb2
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7d7616e306e2ba86fe0e64c3b521b762
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6285-5616
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-7877-7395
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-3032-014X
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_de7a2c4e3111a7d7f83dc4fac1f6780b
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8ce6cce55a5a5e1c81b4652bf3c157ce
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-0377-0807
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_30e251ee6df90a0a81fdf5e289985338
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-9142-1382
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_92425112e637c9954585cc7ad88f3332
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-7162-5871
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_81da0ef0efaaab3731e82bfabca6a7b9
date 202012
identifier https://pubmed.ncbi.nlm.nih.gov/33659639
https://pubmed.ncbi.nlm.nih.gov/PMC7803339
https://doi.org/10.1212/nxg.0000000000000534
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/44855
https://portal.issn.org/resource/ISSN/2376-7839
language English
source https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/
title New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8577
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_abd79932a6d3df66c2c2a45d8adf2907
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10325
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10542
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8539
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5460341

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8N9I0

Total number of triples: 48.