Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1878-7479
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias ; day:3 ; month:1 ; year:2019 ; pages:1-24
Neurotherapeutics ; (3.1.2019), 1-24
- Urheber
-
Buijsen, Ronald A.M
Toonen, Lodewijk J.A
Gardiner, Sarah L.
Roon-Mom, Willeke M.C. van
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1007/s13311-018-00696-y
- URN
-
urn:nbn:de:101:1-2019020900303705572515
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:52 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Buijsen, Ronald A.M
- Toonen, Lodewijk J.A
- Gardiner, Sarah L.
- Roon-Mom, Willeke M.C. van
- SpringerLink (Online service)
Ähnliche Objekte (12)
Genetics of Depression: Progress at Last
Progress in population genetics and human evolution
Progress in clinical genetics of prostate cancer
Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31)
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms
The natural breakthrough: phytochemicals as potent therapeutic agents against spinocerebellar ataxia type 3
Recent progress in genetics of adolescent idiopathic scoliosis
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological Mechanisms
Spinocerebellar ataxia type 31 (SCA31)
Expansion, mosaicism and interruption: mechanisms of the CAG repeat mutation in spinocerebellar ataxia type 1
Genetics of Depression: Progress at Last
Progress in population genetics and human evolution
Progress in clinical genetics of prostate cancer
Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31)
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms
The natural breakthrough: phytochemicals as potent therapeutic agents against spinocerebellar ataxia type 3
Recent progress in genetics of adolescent idiopathic scoliosis
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological Mechanisms
Spinocerebellar ataxia type 31 (SCA31)
Expansion, mosaicism and interruption: mechanisms of the CAG repeat mutation in spinocerebellar ataxia type 1
Genetics of Depression: Progress at Last
Progress in population genetics and human evolution
Progress in clinical genetics of prostate cancer
Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31)
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms
The natural breakthrough: phytochemicals as potent therapeutic agents against spinocerebellar ataxia type 3
Recent progress in genetics of adolescent idiopathic scoliosis
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological Mechanisms
Spinocerebellar ataxia type 31 (SCA31)