Molecular basis of the Kell (K1) phenotype
S Lee(New York Blood Center), C M Redman(New York Blood Center), Xu Wu(Loyola University Chicago), Teresa Zelinski(Research Manitoba), M.E. Reid(New York Blood Center)
Cited by 138
Related Papers
Deficiency of Innate and Acquired Immunity Caused by an <i>IKBKB</i> Mutation
|New England Journal of Medicine|2013|184
Blood group terminology 2004: from the International Society of Blood Transfusion committee on terminology for red cell surface antigens
|Vox Sanguinis|2004|180
Blood Group Terminology 1995: ISBT Working Party on Terminology for Red Cell Surface Antigens
|Vox Sanguinis|1995|139
Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome
|The American Journal of Human Genetics|2009|128
GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome
|The American Journal of Human Genetics|2012|124