Type 2 oculocutaneous albinism (OCA2; MIM# 2032000)—an autosomal recessive disorder in which the biosynthesis of melanin pigment is reduced in the skin, hair and eyes—is associated with the ocular ...
Explore the genetic architecture of pigmentation, revealing insights into the HERC2 and OCA2 genes across populations. The last decade has witnessed important advances in our understanding of the ...
In the most elementary form, the inheritance of eye color is classified as a Mendelian trait. 1 On the basis of the observation of more than two phenotypes, eye color has a more complex pattern of ...
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