TCIRG1 associated Congenital Neutropenia

Severe congenital neutropenia (SCN) is a rare hematopoietic disorder, with estimated incidence of 1 in 200,000 individuals of European descent, many cases of which are inherited in an autosomal dominant pattern. Despite the fact that several causal genes have been identified, the genetic basis for &...

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Bibliographische Detailangaben
Hauptverfasser: Makaryan, Vahagn, Rosenthal, Elisabeth A., Bolyard, Audrey Anna, Kelley, Merideth L., Below, Jennifer E., Bamshad, Michael J., Bofferding, Kathryn M., Smith, Joshua D., Buckingham, Kati, Boxer, Laurence A., Skokowa, Julia, Welte, Karl, Nickerson, Deborah A., Jarvik, Gail P., Dale, David C.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2014
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4055522/
https://ncbi.nlm.nih.gov/pubmed/24753205
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22563
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