3 Einträge gefunden

1. CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures

   1. Sargolzaeiaval, Forough
   2. Zhang, Jiaming
   3. Schleit, Jennifer
   4. Lessel, Davor
   5. Kubisch, Christian
   6. Precioso, Debora R
   7. Sillence, David

   2018 - Forschungsinformationssystem des UKE - frei zugänglich
2. Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry

   1. Saha, Bidisha
   2. Lessel, Davor
   3. Nampoothiri, Sheela
   4. Rao, Anuradha S
   5. Hisama, Fuki M
   6. Peter, Dincy
   7. Bennett, Chris

   2013 - Forschungsinformationssystem des UKE - frei zugänglich
3. Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.

   1. Hisama, Fuki M
   2. Lessel, Davor
   3. Leistritz, Dru
   4. Friedrich, Katrin
   5. McBride, Kim L
   6. Pastore, Matthew T
   7. Gottesman, Gary S

   2011 - Forschungsinformationssystem des UKE