Associated Papers
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons.
Bolze A et al.
Proceedings of the National Academy of Sciences of the United States of America, 2018
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
Bolze A et al.
Science (new York, N.y.), 2013
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