2 Einträge gefunden

1. SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden

   1. Yilmaz, Rüstem
   2. Müller, Kathrin
   3. Brenner, David
   4. Volk, Alexander E
   5. Borck, Guntram
   6. Hermann, Andreas
   7. Meitinger, Thomas

   2020 - Forschungsinformationssystem des UKE
2. Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

   1. Müller, Kathrin
   2. Andersen, Peter M
   3. Hübers, Annemarie
   4. Marroquin, Nicolai
   5. Volk, Alexander E
   6. Danzer, Karin M
   7. Meitinger, Thomas

   2014 - Forschungsinformationssystem des UKE