Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.

Sickle cell disease (SCD) is the most common monogenic disorder in the world. Notably, there is extensive clinical heterogeneity in SCD that cannot be fully accounted for by known factors, and in particular, the extent to which the phenotypic diversity of SCD can be explained by genetic variation ha...

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Detalhes bibliográficos
Publicado no:Am J Hematol
Main Authors: Bao, Erik L., Lareau, Caleb A., Brugnara, Carlo, Fulcher, Isabel, Barau, Caroline, Moutereau, Stephane, Habibi, Anoosha, Badaoui, Bouchra, Berkenou, Jugurtha, Bartolucci, Pablo, Galactéros, Frédéric, Platt, Orah S., Mahaney, Michael, Sankaran, Vijay G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6449202/
https://ncbi.nlm.nih.gov/pubmed/30680775
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.25421
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