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 &...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: 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.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2014
Onderwerpen:
Article
Online toegang: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
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items