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- Q86123986 description "article scientifique publié en 2014" @default.
- Q86123986 description "artículu científicu espublizáu n'ochobre de 2014" @default.
- Q86123986 description "scientific article published on 16 October 2014" @default.
- Q86123986 description "wetenschappelijk artikel" @default.
- Q86123986 description "наукова стаття, опублікована в жовтні 2014" @default.
- Q86123986 name "A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8" @default.
- Q86123986 name "A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8" @default.
- Q86123986 type Item @default.
- Q86123986 label "A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8" @default.
- Q86123986 label "A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8" @default.
- Q86123986 prefLabel "A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8" @default.
- Q86123986 prefLabel "A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8" @default.
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- Q86123986 P1433 Q86123986-87D99743-8252-491F-820F-DD39CC15EC2B @default.
- Q86123986 P1476 Q86123986-02446AB3-2F61-4E70-9E1C-63F4DD076B9D @default.
- Q86123986 P2093 Q86123986-02B37CCB-62BD-45B8-945F-E6ECA85AF88A @default.
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- Q86123986 P2093 Q86123986-2128DED8-9F6A-4B0F-85CA-6F7A46EDFB9F @default.
- Q86123986 P2093 Q86123986-7212051F-E759-4BEB-A8EE-5F0DF0AD7679 @default.
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- Q86123986 P2093 Q86123986-D143EB04-6B7E-4D0D-BDB4-FE8746E78413 @default.
- Q86123986 P2093 Q86123986-D9F0EBB6-A924-4060-8A4B-3BC253F0CD08 @default.
- Q86123986 P304 Q86123986-CADAE1AD-1B0F-4CF9-8207-3CF23101FB5D @default.
- Q86123986 P31 Q86123986-ED44E3E5-41DC-4A4B-924F-B7F45AC487DC @default.
- Q86123986 P356 Q86123986-4D2A7CA9-8A21-420B-A724-D25291587364 @default.
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- Q86123986 P50 Q86123986-FB98E423-89DF-45E4-B535-A359BF6CF9F6 @default.
- Q86123986 P577 Q86123986-45EFDAD1-EDC3-4737-B227-FD616762A7FA @default.
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- Q86123986 P921 Q86123986-E0FDBBBF-C8AE-4BD5-BE65-96ABC1E4CAB7 @default.
- Q86123986 P356 J.JNS.2014.10.018 @default.
- Q86123986 P698 25454649 @default.
- Q86123986 P1104 "+3" @default.
- Q86123986 P1433 Q6296168 @default.
- Q86123986 P1476 "A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8" @default.
- Q86123986 P2093 "Amir Jahic" @default.
- Q86123986 P2093 "Andrea Bier" @default.
- Q86123986 P2093 "Friedmar Kreuz" @default.
- Q86123986 P2093 "Jana Fiedler" @default.
- Q86123986 P2093 "Jens Plaschke" @default.
- Q86123986 P2093 "Manuela Rieger" @default.
- Q86123986 P2093 "Pia Zacher" @default.
- Q86123986 P2093 "Silke Reif" @default.
- Q86123986 P2093 "Stefan Krüger" @default.
- Q86123986 P304 "372-374" @default.
- Q86123986 P31 Q13442814 @default.
- Q86123986 P356 "10.1016/J.JNS.2014.10.018" @default.
- Q86123986 P433 "1-2" @default.
- Q86123986 P478 "347" @default.
- Q86123986 P50 Q47417662 @default.
- Q86123986 P577 "2014-10-16T00:00:00Z" @default.
- Q86123986 P698 "25454649" @default.
- Q86123986 P921 Q657516 @default.