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A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2)

โœ Scribed by Kato, Atsushi; Fukai, Kazuyoshi; Oiso, Naoki; Hosomi, Naoko; Saitoh, Shinji; Wada, Takahito; Shimizu, Hiroshi; Ishii, Masamitsu

Book ID
119561007
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
232 KB
Volume
31
Category
Article
ISSN
0923-1811

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