|  Help  |  About  |  Contact Us

Publication : A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.

First Author  Ballew BJ Year  2013
Journal  PLoS Genet Volume  9
Issue  8 Pages  e1003695
PubMed ID  24009516 Mgi Id 
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

1 Bio Entities

Trail: Publication

0 Expression