Detalhe da pesquisa
1.
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.
PLoS Genet
; 9(8): e1003695, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24009516