Dagan Jenkins  PhD

Lecturer in Molecular Medicine.  UCL Institute of Child Health, 30 Guilford Street London WC1N 1EH.   

Rare skeletal disorders, especially those caused by mutations affecting primary cilia, phospholipid signaling and ribosome biogenesis – eg, recent discovery of Carpenter, Lenz-Majewski, 3MC and Turner syndromes;  mouse and zebrafish models.

w:  https://iris.ucl.ac.uk/iris/browse/profile?upi=DJENK95

https://www.ucl.ac.uk/ich/research/genetics-genomic-medicine/experimental-personalised-medicine/research-groups/dr-dagan-jenkins

e:   d.jenkins@ucl.ac.uk

t:   +44 (0)20 7905 2838