2 Einträge gefunden

1. A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.

   1. Neu, Axel
   2. Eiselt, Michele
   3. Paul, Matthias
   4. Sauter, Kathrin
   5. Stallmeyer, Birgit
   6. Isbrandt, Dirk
   7. Schulze-Bahr, Eric

   2010 - Forschungsinformationssystem des UKE
2. Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I.

   1. Kruse, Martin
   2. Schulze-Bahr, Eric
   3. Corfield, Valerie
   4. Beckmann, Alf
   5. Stallmeyer, Birgit
   6. Kurtbay, Güven
   7. Ohmert, Iris

   2009 - Forschungsinformationssystem des UKE