## Oculocutaneous albinism type II (OCA2) is the most common form of albinism in humans. OCA2 has been previously associated with mutations of the P gene, the human homologue to the murine pink-eyed dilution gene. The P gene encodes a 110 kDa protein containing 12 potential membrane spanning domain
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Amelanotic melanoma in a child with oculocutaneous albinism
โ Scribed by Terenziani, Monica ;Spreafico, Filippo ;Serra, Annalisa ;Podda, Marta ;Cereda, Stefano ;Belli, Filiberto
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
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- Volume
- 41
- Category
- Article
- ISSN
- 0098-1532
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