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1 Ergebnisse
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A recessive Na v 1.4 mutation underlies congenital myasthen..:
Habbout, Karima
;
Poulin, Hugo
;
Rivier, Francois
...
info:eu-repo/semantics/altIdentifier/pmid/26659129. , 2016
Link:
https://hal.umontpellier.fr/hal-01817830
RT Journal T1
A recessive Na v 1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis
UL https://suche.suub.uni-bremen.de/peid=base-ftccsdartic:oai:HAL:hal-01817830v1&Exemplar=1&LAN=DE A1 Habbout, Karima A1 Poulin, Hugo A1 Rivier, Francois A1 Giuliano, Serena A1 Sternberg, Damien A1 Fontaine, Bertrand A1 Eymard, Bruno A1 Morales, Raul Juntas A1 Echenne, Bernard A1 King, Louise A1 Hanna, Michael A1 Männikkö, Roope A1 Chahine, Mohamed A1 Nicole, Sophie A1 Bendahhou, Saïd PB HAL CCSD; American Academy of Neurology YR 2016 K1 [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC] K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics JF info:eu-repo/semantics/altIdentifier/pmid/26659129 LK http://dx.doi.org/https://hal.umontpellier.fr/hal-01817830 DO https://hal.umontpellier.fr/hal-01817830 SF ELIB - SuUB Bremen
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