Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies) - Aix-Marseille Université Access content directly
Journal Articles Human Genetics Year : 2018

Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)

Nuria Bramswig
  • Function : Author
Aida Bertoli-Avella
Aida Al Aqeel
  • Function : Author
Amal Alhashem
  • Function : Author
Nouriya Al-Sannaa
  • Function : Author
Maissa Bah
  • Function : Author
Katharina Bröhl
  • Function : Author
Diane Doummar
  • Function : Author
  • PersonId : 953196
Nadja Ehmke
  • Function : Author
Hasnaa Elbendary
  • Function : Author
Delphine Heron
  • Function : Author
  • PersonId : 906967
Kiely James
  • Function : Author
Boris Keren
Samira Ismail
  • Function : Author
Mahmoud Issa
  • Function : Author
Michèle Mayer
  • Function : Author
Jennifer Mcevoy-Venneri
  • Function : Author
Cyril Mignot
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  • PersonId : 934439
Sarar Mohamed
  • Function : Author
Arndt Rolfs
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  • PersonId : 886341
Abdelrahim Abdrabou Sadek
  • Function : Author
Lara Segebrecht
  • Function : Author
Valentina Stanley
  • Function : Author
Camille Trautman
  • Function : Author
Tim M Strom
  • Function : Author
  • PersonId : 982618
Maha Zaki
  • Function : Author
Peter Bauer
  • Function : Author
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Dates and versions

hal-01932799 , version 1 (06-10-2023)

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Nuria Bramswig, Aida Bertoli-Avella, Beate Albrecht, Aida Al Aqeel, Amal Alhashem, et al.. Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies). Human Genetics, 2018, 137 (9), pp.753 - 768. ⟨10.1007/s00439-018-1929-5⟩. ⟨hal-01932799⟩
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