## 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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Two novel splice mutations of P gene in a Thai-Chinese patient with oculocutaneous albinism type II (OCA2)
โ Scribed by Wattanasirichaigoon, Duangrurdee; Suwannarat, Pim; Thongpradit, Supranee
- Book ID
- 119293327
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 653 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0923-1811
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