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ALBINISM, OCULOCUTANEOUS, TYPE V

Known as: OCA5 
 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal recessive inheritanceNystagmusPhotophobia

Papers overview

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2017
2017
Metal availability, soil nutrient, and enzyme activity in response to application of organic amendments in Cd-contaminated soil
The study investigated the effects of organic amendments: green tea amendment (GTA) and oil cake amendment (OCA) on Cd… Expand
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Review
2014
Review
2014
Mutational Analysis of Oculocutaneous Albinism: A Compact Review
Oculocutaneous albinism (OCA) is an autosomal recessive disorder caused by either complete lack of or a reduction of melanin… Expand
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Review
2014
Review
2014
Increasing the complexity: new genes and new types of albinism
Albinism is a rare genetic condition globally characterized by a number of specific deficits in the visual system, resulting in… Expand
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2013
2013
OCA5, a novel locus for non‐syndromic oculocutaneous albinism, maps to chromosome 4q24
To the Editor : Oculocutaneous albinism (OCA) is a genetically heterogeneous disorder manifested as a loss of pigmentation in the… Expand
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