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Dual Molecular Effects of Dominant RORA Mutations Cause Two..:
Guissart, Claire
;
Latypova, Xenia
;
Rollier, Paul
...
qt7rq0h7dd. , 2018
Link:
https://escholarship.org/uc/item/7rq0h7dd
RT Journal T1
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt7rq0h7dd&Exemplar=1&LAN=DE A1 Guissart, Claire A1 Latypova, Xenia A1 Rollier, Paul A1 Khan, Tahir N A1 Stamberger, Hannah A1 McWalter, Kirsty A1 Cho, Megan T A1 Kjaergaard, Susanne A1 Weckhuysen, Sarah A1 Lesca, Gaetan A1 Besnard, Thomas A1 Õunap, Katrin A1 Schema, Lynn A1 Chiocchetti, Andreas G A1 McDonald, Marie A1 de Bellescize, Julitta A1 Vincent, Marie A1 Van Esch, Hilde A1 Sattler, Shannon A1 Forghani, Irman A1 Thiffault, Isabelle A1 Freitag, Christine M A1 Barbouth, Deborah Sara A1 Cadieux-Dion, Maxime A1 Willaert, Rebecca A1 Sacoto, Maria J Guillen A1 Safina, Nicole P A1 Dubourg, Christèle A1 Grote, Lauren A1 Carré, Wilfrid A1 Saunders, Carol A1 Pajusalu, Sander A1 Farrow, Emily A1 Boland, Anne A1 Karlowicz, Danielle Hays A1 Deleuze, Jean-François A1 Wojcik, Monica H A1 Pressman, Rena A1 Isidor, Bertrand A1 Vogels, Annick A1 Van Paesschen, Wim A1 Al-Gazali, Lihadh A1 Shamsi, Aisha Mohamed Al A1 Claustres, Mireille A1 Pujol, Aurora A1 Sanders, Stephan J A1 Rivier, François A1 Leboucq, Nicolas A1 Cogné, Benjamin A1 Sasorith, Souphatta A1 Sanlaville, Damien A1 Retterer, Kyle A1 Odent, Sylvie A1 Katsanis, Nicholas A1 Bézieau, Stéphane A1 Koenig, Michel A1 Davis, Erica E A1 Pasquier, Laurent A1 Küry, Sébastien PB eScholarship, University of California YR 2018 K1 Biological Sciences K1 Bioinformatics and Computational Biology K1 Biomedical and Clinical Sciences K1 Genetics K1 Intellectual and Developmental Disabilities (IDD) K1 Neurodegenerative K1 Neurosciences K1 Pediatric K1 Rare Diseases K1 Brain Disorders K1 Autism K1 Mental Health K1 2.1 Biological and endogenous factors K1 Aetiology K1 Neurological K1 Adolescent K1 Adult K1 Aged K1 80 and over K1 Alleles K1 Animals K1 Autistic Disorder K1 Brain K1 Cerebellar Ataxia K1 Child K1 Preschool K1 DNA Copy Number Variations K1 Disease Models K1 Animal K1 Female K1 Genes K1 Dominant K1 Genetic Complementation Test K1 Humans K1 Intellectual Disability K1 Larva K1 Magnetic Resonance Imaging K1 Male K1 Middle Aged K1 Mutation K1 Missense K1 Nuclear Receptor Subfamily 1 K1 Group F K1 Member 1 K1 Purkinje Cells K1 Syndrome K1 Zebrafish K1 RORA K1 autistic features JF qt7rq0h7dd LK http://dx.doi.org/https://escholarship.org/uc/item/7rq0h7dd DO https://escholarship.org/uc/item/7rq0h7dd SF ELIB - SuUB Bremen
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