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ALBINISM, OCULOCUTANEOUS, TYPE VI

Known as: OCA6 
National Institutes of Health

Papers overview

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2019
2019
Non‐syndromic oculocutaneous albinism (nsOCA) is a group of genetically heterogeneous autosomal recessive disorders with complete… 
2019
2019
ABSTRACT Oculocutaneous albinism (OCA) is a heterogeneous and autosomal recessive hypopigmentation disorder, which is caused by… 
2017
2017
Oculocutaneous albinism (OCA) is characterized by hypopigmentation of the skin, hair and eye, and by ophthalmologic abnormalities… 
Review
2017
Review
2017
Purpose of review Childhood skin cancers are relatively rare and may indicate an underlying genetic disorder. The increasing… 
2016
2016
To take out a personal subscription, please click here More information about Pigment Cell & Melanoma Research at www.pigment.org… 
2016
2016
K+-dependent Na+/Ca2+ exchangers belong to the solute carrier 24 (SLC24A1–5) gene family of membrane transporters. Five different… 
Review
2014
Review
2014
Albinism is a rare genetic condition globally characterized by a number of specific deficits in the visual system, resulting in… 
Review
2014
Review
2014
Oculocutaneous albinism (OCA) is an autosomal recessive disorder caused by either complete lack of or a reduction of melanin… 
Highly Cited
2013
Highly Cited
2013
Oculocutaneous albinism (OCA) is a heterogeneous and autosomal recessive disorder with hypopigmentation in the eye, hair, and…