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pro vyhledávání: '"Lola Tóth"'
Autor:
Beáta Fábos, Katalin Farkas, Lola Tóth, Adrienn Sulák, Kornélia Tripolszki, Mariann Tihanyi, Réka Németh, Krisztina Vas, Zsanett Csoma, Lajos Kemény, Márta Széll, Nikoletta Nagy
Publikováno v:
European Journal of Medical Research, Vol 22, Iss 1, Pp 1-8 (2017)
Abstract Background Oculocutaneous albinism (OCA) is a clinically and genetically heterogenic group of pigmentation abnormalities characterized by variable hair, skin, and ocular hypopigmentation. Six known genes and a locus on human chromosome 4q24
Externí odkaz:
https://doaj.org/article/bb51dfc20d624efebb356ce4b7cc9918