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ALBINISM, OCULOCUTANEOUS, TYPE VI

Known as: OCA6 
National Institutes of Health

Papers overview

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