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| Title : The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study - Krenn_2022_J.Neurol__ |
| Author(s) : Krenn M , Sener M , Rath J , Zulehner G , Keritam O , Wagner M , Laccone F , Iglseder S , Marte S , Baumgartner M , Eisenkolbl A , Liechtenstein C , Rudnik S , Quasthoff S , Grinzinger S , Spenger J , Wortmann SB , Loscher WN , Zimprich F , Kellersmann A , Rappold M , Bernert G , Freilinger M , Cetin H |
| Ref : Journal of Neurology , : , 2022 |
| Abstract : Krenn_2022_J.Neurol__ |
| ESTHER : Krenn_2022_J.Neurol__ |
| PubMedSearch : Krenn_2022_J.Neurol__ |
| PubMedID: 36308527 |
| Title : Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance - Finsterer_2012_J.Neurol.Sci_318_1 |
| Author(s) : Finsterer J , Loscher W , Quasthoff S , Wanschitz J , Auer-Grumbach M , Stevanin G |
| Ref : Journal of Neurology Sci , 318 :1 , 2012 |
| Abstract : Finsterer_2012_J.Neurol.Sci_318_1 |
| ESTHER : Finsterer_2012_J.Neurol.Sci_318_1 |
| PubMedSearch : Finsterer_2012_J.Neurol.Sci_318_1 |
| PubMedID: 22554690 |
| Gene_locus related to this paper: human-SPG21 |