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Exome sequencing reveals a novel CWF19L1 mutation associate..:
Evers, Christina
;
Kaufmann, Lilian
;
Seitz, Angelika
...
American Journal of Medical Genetics Part A. 170 (2016) 6 - p. 1502-1509 , 2016
Link:
https://doi.org/10.1002/ajmg.a.37632
RT Journal T1 <Title>Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.37632&Exemplar=1&LAN=DE A1 Evers, Christina A1 Kaufmann, Lilian A1 Seitz, Angelika A1 Paramasivam, Nagarajan A1 Granzow, Martin A1 Karch, Stephanie A1 Fischer, Christine A1 Hinderhofer, Katrin A1 Gdynia, Georg A1 Elsässer, Michael A1 Pinkert, Stefan A1 Schlesner, Matthias A1 Bartram, Claus R. A1 Moog, Ute PB Wiley YR 2016 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 170 IS 6 SP 1502 OP 1509 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.37632 DO https://doi.org/10.1002/ajmg.a.37632 SF ELIB - SuUB Bremen
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