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Genetic variants in components of the NALCN–UNC80–UNC79 ion..:
Bramswig, Nuria
;
Bertoli-Avella, Aida
;
Albrecht, Beate
...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00439-018-1929-5. , 2018
Link:
https://amu.hal.science/hal-01932799
RT Journal T1
Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)
UL https://suche.suub.uni-bremen.de/peid=base-ftunivparis:oai:HAL:hal-01932799v1&Exemplar=1&LAN=DE A1 Bramswig, Nuria A1 Bertoli-Avella, Aida A1 Albrecht, Beate A1 Al Aqeel, Aida A1 Alhashem, Amal A1 Al-Sannaa, Nouriya A1 Bah, Maissa A1 Bröhl, Katharina A1 Depienne, Christel A1 Dorison, Nathalie A1 Doummar, Diane A1 Ehmke, Nadja A1 Elbendary, Hasnaa A1 Gorokhova, Svetlana A1 Heron, Delphine A1 Horn, Denise A1 James, Kiely A1 Keren, Boris A1 Kuechler, Alma A1 Ismail, Samira A1 Issa, Mahmoud A1 Marey, Isabelle A1 Mayer, Michèle A1 Mcevoy-Venneri, Jennifer A1 Mégarbané, André A1 Mignot, Cyril A1 Mohamed, Sarar A1 Nava, Caroline A1 Philip, Nicole A1 Mignon-Ravix, Cecile A1 Rolfs, Arndt A1 Sadek, Abdelrahim Abdrabou A1 Segebrecht, Lara A1 Stanley, Valentina A1 Trautman, Camille A1 Valence, Stephanie A1 Villard, Laurent A1 Wieland, Thomas A1 Engels, Hartmut A1 Strom, Tim, M A1 Zaki, Maha A1 Gleeson, Joseph A1 Lüdecke, Hermann-Josef A1 Bauer, Peter A1 Wieczorek, Dagmar PB HAL CCSD; Springer Verlag YR 2018 K1 [SDV]Life Sciences [q-bio] K1 [SDV.GEN]Life Sciences [q-bio]/Genetics K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1007/s00439-018-1929-5 LK http://dx.doi.org/https://amu.hal.science/hal-01932799 DO https://amu.hal.science/hal-01932799 SF ELIB - SuUB Bremen
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