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Year | Number of Results |
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1994 | 1 |
1995 | 2 |
2024 | 0 |
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An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids.
Am J Hum Genet. 1995 Mar;56(3):586-91.
Am J Hum Genet. 1995.
PMID: 7887411
Free PMC article.
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism.
Durham-Pierre D, Gardner JM, Nakatsu Y, King RA, Francke U, Ching A, Aquaron R, del Marmol V, Brilliant MH.
Durham-Pierre D, et al.
Nat Genet. 1994 Jun;7(2):176-9. doi: 10.1038/ng0694-176.
Nat Genet. 1994.
PMID: 7920637
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Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2).
Spritz RA, Fukai K, Holmes SA, Luande J.
Spritz RA, et al.
Am J Hum Genet. 1995 Jun;56(6):1320-3.
Am J Hum Genet. 1995.
PMID: 7762554
Free PMC article.
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