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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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| Autori principali: | , , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2014
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| Soggetti: | |
| Accesso online: | 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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