2 Einträge gefunden

1. A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly.

   1. Kakar, Naseebullah
   2. Goebel, Ingrid
   3. Daud, Shakeela
   4. Nürnberg, Gudrun
   5. Agha, Noor
   6. Ahmad, Adeel
   7. Nürnberg, Peter

   2012 - Forschungsinformationssystem des UKE
2. Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts.

   1. Ahmad, Adeel
   2. Daud, Shakeela
   3. Kakar, Naseebullah
   4. Nürnberg, Gudrun
   5. Nürnberg, Peter
   6. Babar, Masroor Ellahi
   7. Thoenes, Michaela

   2011 - Forschungsinformationssystem des UKE - frei zugänglich