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- Q99631566 description "artículu científicu espublizáu n'agostu de 2020" @default.
- Q99631566 description "scientific article published on 31 August 2020" @default.
- Q99631566 description "wetenschappelijk artikel" @default.
- Q99631566 description "наукова стаття, опублікована 31 серпня 2020" @default.
- Q99631566 description "գիտական հոդված հրատարակված 2020 թվականի օգոստոսի 31-ին" @default.
- Q99631566 name "The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes" @default.
- Q99631566 name "The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes" @default.
- Q99631566 type Item @default.
- Q99631566 label "The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes" @default.
- Q99631566 label "The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes" @default.
- Q99631566 prefLabel "The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes" @default.
- Q99631566 prefLabel "The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes" @default.
- Q99631566 P1433 Q99631566-5F66C004-DA3B-492F-B2AE-1B8B40F2E1D3 @default.
- Q99631566 P1476 Q99631566-59431F70-D3C6-4CA3-A6A5-2E3EB93CB794 @default.
- Q99631566 P2093 Q99631566-662D2F22-715C-4779-A08E-3A734D9955EA @default.
- Q99631566 P2093 Q99631566-9545E315-AFC4-466B-9964-7E24FE0AA7E7 @default.
- Q99631566 P2093 Q99631566-B2577588-8356-419E-A3E9-FF96D533043F @default.
- Q99631566 P304 Q99631566-3DC9F8E6-B457-45A9-8F1E-F2D207C3C6E4 @default.
- Q99631566 P31 Q99631566-1A008809-23B2-4F93-B6A4-B241A0850DBE @default.
- Q99631566 P356 Q99631566-5A1DEC54-66AE-4E99-9723-51E559ED1CA0 @default.
- Q99631566 P50 Q99631566-10179B06-2170-4B58-A7E8-05516E024933 @default.
- Q99631566 P50 Q99631566-94195973-F360-40DF-967A-F104F9AE4360 @default.
- Q99631566 P577 Q99631566-AA2B96D4-3F2C-4BD2-A8DE-15CA28DFC8ED @default.
- Q99631566 P698 Q99631566-235957A5-D5ED-4C01-B3CB-952709C0AE5D @default.
- Q99631566 P921 Q99631566-056896F6-9E14-4258-84DA-3FEF89A1B2B6 @default.
- Q99631566 P921 Q99631566-1A6517C0-9775-435E-A72F-AB3C79E8176E @default.
- Q99631566 P356 JGM.3265 @default.
- Q99631566 P698 32864802 @default.
- Q99631566 P1433 Q15746377 @default.
- Q99631566 P1476 "The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes" @default.
- Q99631566 P2093 "Afsane Bahrami" @default.
- Q99631566 P2093 "Ali Akbar Momen" @default.
- Q99631566 P2093 "Mohsen Naseri" @default.
- Q99631566 P304 "e3265" @default.
- Q99631566 P31 Q13442814 @default.
- Q99631566 P356 "10.1002/JGM.3265" @default.
- Q99631566 P50 Q55098429 @default.
- Q99631566 P50 Q99631565 @default.
- Q99631566 P577 "2020-08-31T00:00:00Z" @default.
- Q99631566 P698 "32864802" @default.
- Q99631566 P921 Q114049690 @default.
- Q99631566 P921 Q1321884 @default.