Clinical variability and probable founder effect in oculocutaneous albinism type 7.
ARVEILER, Benoit
Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
< Leer menos
Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
Idioma
EN
Article de revue
Este ítem está publicado en
Clinical Genetics. 2020-03-01, vol. 97, n° 3, p. 527-528
Palabras clave en inglés
Albinism
Oculocutaneous
Child
Female
Founder Effect
Genetic Predisposition to Disease
Humans
Membrane Proteins
Pedigree
Receptors
LDL
Centros de investigación