DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
LinksClose Window
References
Albers CA, Paul DS, Schulze H , et al.
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Nat Genet 2012;
44 (4) 435-439 , S1–S2
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.