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1 Ergebnisse
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CAPN1 mutations: Expanding the CAPN1-related phenotype: Fro..:
Shetty, Aakash
;
Gan-Or, Ziv
;
Ashtiani, Setareh
...
European Journal of Medical Genetics. 62 (2019) 12 - p. 103605 , 2019
Link:
https://doi.org/10.1016/j.ejmg.2018.12.010
RT Journal T1
CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2018.12.010&Exemplar=1&LAN=DE A1 Shetty, Aakash A1 Gan-Or, Ziv A1 Ashtiani, Setareh A1 Ruskey, Jennifer A. A1 van de Warrenburg, Bart A1 Wassenberg, Tessa A1 Kamsteeg, Erik-Jan A1 Rouleau, Guy A. A1 Suchowersky, Oksana PB Elsevier BV YR 2019 SN 1769-7212 JF European Journal of Medical Genetics VO 62 IS 12 SP 103605 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2018.12.010 DO https://doi.org/10.1016/j.ejmg.2018.12.010 SF ELIB - SuUB Bremen
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