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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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| 出版年: | Am J Hematol |
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| 主要な著者: | , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
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| 主題: | |
| オンライン･アクセス: | 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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