Title |
Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies) |
|---|---|
Involved |
Nuria C. Bramswig (Verfasser)
Aida M. Bertoli-Avella (Sonstige) Beate Albrecht (Sonstige) Aida I. Al Aqeel (Sonstige)
Amal Alhashem (Sonstige)
Nouriya Al-Sannaa (Sonstige) Maissa Bah (Sonstige) Katharina Bröhl (Sonstige) Christel Depienne (Sonstige) Nathalie Dorison (Sonstige) Diane Doummar (Sonstige) Nadja Ehmke (Sonstige) Hasnaa M. Elbendary (Sonstige) Svetlana Gorokhova (Sonstige) Delphine Héron (Sonstige) Denise Horn (Sonstige) Kiely James (Sonstige) Boris Keren (Sonstige) Alma Kuechler (Sonstige) Samira Ismail (Sonstige) Mahmoud Y. Issa (Sonstige) Isabelle Marey (Sonstige) Michèle Mayer (Sonstige) Jennifer McEvoy-Venneri (Sonstige) Andre Megarbane (Sonstige) Cyril Mignot (Sonstige) Sarar Mohamed (Sonstige) Caroline Nava (Sonstige) Nicole Philip (Sonstige) Cecile Ravix (Sonstige) Arndt Rolfs (Sonstige) Abdelrahim Abdrabou Sadek (Sonstige) Lara Segebrecht (Sonstige) Valentina Stanley (Sonstige) Camille Trautman (Sonstige) Stephanie Valence (Sonstige) Laurent Villard (Sonstige) Thomas Wieland (Sonstige) Hartmut Engels (Sonstige) Tim M. Strom (Sonstige) Maha S. Zaki (Sonstige) Joseph G. Gleeson (Sonstige) Hermann-Josef Lüdecke (Sonstige) Peter Bauer (Sonstige) Dagmar Wieczorek (Sonstige) SpringerLink (Online service) (Sonstige) |
Published in |
Human genetics 137, 9, 23.8.2018, date:9.2018, Seite 753-768 |
Published |
2018 |
Language |
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Country |
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Topic |
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Subject |
Biomedicine. |
DDC notation |
|
Persistent identifier |
urn:nbn:de:101:1-2018110312523362754897 (URN) |
Record ID |
1170501133 |
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