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Autor:
Merideth L. Kelley, Karl Welte, Kati J. Buckingham, Deborah A. Nickerson, Julia Skokowa, Audrey Anna Bolyard, Gail P. Jarvik, Michael J. Bamshad, David C. Dale, Kathryn M. Bofferding, Jennifer E. Below, Laurence A. Boxer, Joshua D. Smith, Elisabeth A. Rosenthal
Publikováno v:
Blood. 122:440-440
Severe congenital neutropenia (SCN) is a rare autosomal dominant hematopoietic disorder with an estimated incidence of 1 in 200,000 for individuals of European descent. Although several causal genes have been identified, the genetic basis for >30% of