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- Q91589213 description "artículu científicu espublizáu n'abril de 2020" @default.
- Q91589213 description "scientific article published on 06 April 2020" @default.
- Q91589213 description "wetenschappelijk artikel" @default.
- Q91589213 description "наукова стаття, опублікована 6 квітня 2020" @default.
- Q91589213 name "Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence" @default.
- Q91589213 name "Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence" @default.
- Q91589213 type Item @default.
- Q91589213 label "Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence" @default.
- Q91589213 label "Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence" @default.
- Q91589213 prefLabel "Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence" @default.
- Q91589213 prefLabel "Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence" @default.
- Q91589213 P1433 Q91589213-EF418C54-8906-4169-A49D-D4E4A6C59C44 @default.
- Q91589213 P1476 Q91589213-E94F72C2-E355-4E2C-AD58-972E7538C386 @default.
- Q91589213 P2093 Q91589213-5750311D-AE94-4A4D-9C9F-6E24180982CE @default.
- Q91589213 P2093 Q91589213-85F80D13-843B-41DD-80BF-FCCD70CBA6E7 @default.
- Q91589213 P31 Q91589213-6EF77087-C668-4BC4-B694-A36195455AA0 @default.
- Q91589213 P356 Q91589213-E59BAD76-F105-43D6-A1E7-49E81B06A65C @default.
- Q91589213 P50 Q91589213-80B0214B-5E06-4D1A-A069-0101B3783122 @default.
- Q91589213 P577 Q91589213-3823C339-FBBE-4090-B629-A09C3C36F5CA @default.
- Q91589213 P698 Q91589213-942201E2-C524-49D3-9B02-E895606ACFF5 @default.
- Q91589213 P921 Q91589213-0E783ED1-C50E-4F33-AB0C-8DD05BC9B730 @default.
- Q91589213 P921 Q91589213-48E11960-DD6B-4C4C-81BB-72FD6F1A613F @default.
- Q91589213 P356 AJMG.A.61579 @default.
- Q91589213 P698 32250532 @default.
- Q91589213 P1433 Q4744254 @default.
- Q91589213 P1476 "Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence" @default.
- Q91589213 P2093 "Hélio van der Linden" @default.
- Q91589213 P2093 "Michael Ferns" @default.
- Q91589213 P31 Q13442814 @default.
- Q91589213 P356 "10.1002/AJMG.A.61579" @default.
- Q91589213 P50 Q87783211 @default.
- Q91589213 P577 "2020-04-06T00:00:00Z" @default.
- Q91589213 P698 "32250532" @default.
- Q91589213 P921 Q114049690 @default.
- Q91589213 P921 Q3508800 @default.