A defect in hematopoietic stem cell migration explains the nonrandom X-chromosome inactivation in carriers of Wiskott-Aldrich syndrome.
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E. Haddad | W. Vainchenker | S. Snapper | C. Lacout | L. Garçon | D. Duménil | F. Louache | S. Sabri | C. Capron | Rym Mzali | Fedor Svinarchouk | A. Foudi | D. Duménil