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1 Ergebnisse
1
Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by ..:
Landouré, Guida
;
Zhu, Peng‐Peng
;
Lourenço, Charles M
...
qt8cg7t7rm. , 2013
Link:
https://escholarship.org/uc/item/8cg7t7rm
RT Journal T1
Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt8cg7t7rm&Exemplar=1&LAN=DE A1 Landouré, Guida A1 Zhu, Peng‐Peng A1 Lourenço, Charles M A1 Johnson, Janel O A1 Toro, Camilo A1 Bricceno, Katherine V A1 Rinaldi, Carlo A1 Meilleur, Katherine G A1 Sangaré, Modibo A1 Diallo, Oumarou A1 Pierson, Tyler M A1 Ishiura, Hiroyuki A1 Tsuji, Shoji A1 Hein, Nichole A1 Fink, John K A1 Stoll, Marion A1 Nicholson, Garth A1 Gonzalez, Michael A A1 Speziani, Fiorella A1 Dürr, Alexandra A1 Stevanin, Giovanni A1 Biesecker, Leslie G A1 Center, for the NIH Intramural Sequencing A1 Accardi, John A1 Landis, Dennis MD A1 Gahl, William A A1 Traynor, Bryan J A1 Marques, Wilson A1 Züchner, Stephan A1 Blackstone, Craig A1 Fischbeck, Kenneth H A1 Burnett, Barrington G PB eScholarship, University of California YR 2013 K1 Biological Sciences K1 Biomedical and Clinical Sciences K1 Genetics K1 Rare Diseases K1 Neurosciences K1 Human Genome K1 Clinical Research K1 Neurodegenerative K1 Aetiology K1 2.1 Biological and endogenous factors K1 Adolescent K1 Amino Acid Sequence K1 Brain K1 Homozygote K1 Humans K1 Intracellular Space K1 Magnetic Resonance Imaging K1 Male K1 Mitochondrial Proteins K1 Molecular Sequence Data K1 Mutation K1 Protein Transport K1 Sequence Alignment K1 Sequence Deletion K1 Spastic Paraplegia K1 Hereditary K1 SPG43 K1 NBIA K1 C19orf12 K1 hereditary spastic paraplegia K1 NIH Intramural Sequencing Center K1 Clinical Sciences K1 Genetics & Heredity JF qt8cg7t7rm LK http://dx.doi.org/https://escholarship.org/uc/item/8cg7t7rm DO https://escholarship.org/uc/item/8cg7t7rm SF ELIB - SuUB Bremen
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