## 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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P▪12 PGD for oculocutaneous albinism type II
✍ Scribed by T Sharapova; S Rechitsky; R Ozen; K Laziuk; I Barsky; O Verlinsky; Y Verlinsky
- Book ID
- 119612255
- Publisher
- Reproductive Healthcare Ltd
- Year
- 2005
- Tongue
- English
- Weight
- 104 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1472-6491
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