Clinical variability and probable founder effect in oculocutaneous albinism type 7.

Clin Genet

Reference Centre for Genodermatoses and Rare Skin Disease (MAGEC) and Department of Dermatology, Filière Maladies Rares Dermatologiques (FIMARAD), ERN-Skin Hôpital Necker-Enfants Malades, Université de Paris-Centre, Paris, France.

Published: March 2020

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Source
http://dx.doi.org/10.1111/cge.13655DOI Listing

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