Newly published research provides the first demonstration of how a genetic mutation associated with a common form of albinism leads to the lack of melanin pigments that characterizes the condition. About 1 in 40,000 people worldwide have type 2 oculocutaneous albinism, which has symptoms of…
Source:New research unlocks a mystery of albinism
Tuesday, December 16, 2014
New research unlocks a mystery of albinism
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