Delineating the genetic heterogeneity of OCA in Hungarian patients

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 have been implicated in the etiology of isolated OCA forms...

Descripción completa

Detalles Bibliográficos
Autores principales: Fábos, Beáta, Farkas, Katalin, Tóth, Lola, Sulák, Adrienn, Tripolszki, Kornélia, Tihanyi, Mariann, Németh, Réka, Vas, Krisztina, Csoma, Zsanett, Kemény, Lajos, Széll, Márta, Nagy, Nikoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477306/
https://www.ncbi.nlm.nih.gov/pubmed/28629449
http://dx.doi.org/10.1186/s40001-017-0262-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477306/
https://www.ncbi.nlm.nih.gov/pubmed/28629449
http://dx.doi.org/10.1186/s40001-017-0262-0

Ejemplares similares