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1 Ergebnisse
1
A Novel c.3636-4 A>G Mutation in the CCDC88C Plays a Causat..:
Chai, Senmao
;
Liu, Deyang
;
Liu, Yajing
.
Human Heredity. 88 (2023) 1 - p. 91-97 , 2023
Link:
https://doi.org/10.1159/000534692
RT Journal T1
A Novel c.3636-4 A>G Mutation in the CCDC88C Plays a Causative Role in Familial Spinocerebellar Ataxia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1159_000534692&Exemplar=1&LAN=DE A1 Chai, Senmao A1 Liu, Deyang A1 Liu, Yajing A1 Sang, Ming PB S. Karger AG YR 2023 SN 0001-5652 SN 1423-0062 JF Human Heredity VO 88 IS 1 SP 91 OP 97 LK http://dx.doi.org/https://doi.org/10.1159/000534692 DO https://doi.org/10.1159/000534692 SF ELIB - SuUB Bremen
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