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- Q73210149 description "artículu científicu espublizáu en xunu de 2000" @default.
- Q73210149 description "im Juni 2000 veröffentlichter wissenschaftlicher Artikel" @default.
- Q73210149 description "scientific article published on 01 June 2000" @default.
- Q73210149 description "wetenschappelijk artikel" @default.
- Q73210149 description "наукова стаття, опублікована в червні 2000" @default.
- Q73210149 name "[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA]" @default.
- Q73210149 name "[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA]" @default.
- Q73210149 type Item @default.
- Q73210149 label "[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA]" @default.
- Q73210149 label "[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA]" @default.
- Q73210149 prefLabel "[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA]" @default.
- Q73210149 prefLabel "[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA]" @default.
- Q73210149 P1433 Q73210149-F2D9369F-9771-4F76-9C6A-8C6EAB692D51 @default.
- Q73210149 P1476 Q73210149-5083C0EB-31D3-4FA7-86A5-5E213BA2F109 @default.
- Q73210149 P2093 Q73210149-27E47B9C-69AE-4E2B-85B4-3392346770FB @default.
- Q73210149 P2093 Q73210149-518A8985-434E-4D5F-A282-9DCF83B7A047 @default.
- Q73210149 P2093 Q73210149-6F0B5271-86E2-49E2-A941-AE24A904D047 @default.
- Q73210149 P2093 Q73210149-8619E43B-DB1F-4127-8409-15601AA7AEF3 @default.
- Q73210149 P2093 Q73210149-EB36A509-12FA-49D0-8CC3-49B1C90B58BC @default.
- Q73210149 P304 Q73210149-254822DE-1672-4F81-A9C7-089F54673616 @default.
- Q73210149 P31 Q73210149-0CD621D9-84B5-49BC-BE82-9F1FA3BBCB11 @default.
- Q73210149 P433 Q73210149-52F268B4-8400-465C-B7EA-4386FBCCF7CA @default.
- Q73210149 P478 Q73210149-12A1B95F-50EC-4B52-90E4-6EF552432D89 @default.
- Q73210149 P577 Q73210149-882DDE0F-DDED-46FD-B70B-30781885BE81 @default.
- Q73210149 P698 Q73210149-3209983D-EA48-4AAE-8A44-7022872242EB @default.
- Q73210149 P921 Q73210149-048FFD8D-50FA-4C9B-BE99-9A65EF2A9D5D @default.
- Q73210149 P921 Q73210149-52DEEB9D-EC65-4847-B01D-BE816BA42442 @default.
- Q73210149 P698 11086401 @default.
- Q73210149 P1433 Q15753493 @default.
- Q73210149 P1476 "[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA]" @default.
- Q73210149 P2093 "Jinnai K" @default.
- Q73210149 P2093 "Koide R" @default.
- Q73210149 P2093 "Mitani M" @default.
- Q73210149 P2093 "Takahashi K" @default.
- Q73210149 P2093 "Tsuji S" @default.
- Q73210149 P304 "600-604" @default.
- Q73210149 P31 Q13442814 @default.
- Q73210149 P433 "6" @default.
- Q73210149 P478 "40" @default.
- Q73210149 P577 "2000-06-01T00:00:00Z" @default.
- Q73210149 P698 "11086401" @default.
- Q73210149 P921 Q270421 @default.
- Q73210149 P921 Q847057 @default.