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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Am J Hematol
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2019
Aiheet:
Article
Linkit: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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