article · European Journal of Medical Genetics

Co-occurrence of oculocutaneous albinism type 2 and mild sickle cell disease explained by HbS/βthal genotype in an individual from the Democratic Republic of Congo

R Aquaron
Benoı̂t Arveiler
Joseph K. Kelekele
Catherine Badens
Nathalie Bonello‐Palot
Eulalie Lasseaux
Léon Tshilolo

20222 citationsUniversité de Kinshasa (UNIKIN)

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Research topics

melanin and skin pigmentation
RNA regulation and disease
Hemoglobinopathies and Related Disorders

Sustainable Development Goals

1No Poverty

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DOI: 10.1016/j.ejmg.2022.104594

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