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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Bibliografiska uppgifter
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2014
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Article
Länkar: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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