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22. Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism. King RA, Mentink MM, Oetting WS. Mol Biol Med; 1991 Feb; 8(1):19-29. PubMed ID: 1943686 [Abstract] [Full Text] [Related]
23. Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism. King RA, Townsend D, Oetting W, Summers CG, Olds DP, White JG, Spritz RA. J Clin Invest; 1991 Mar; 87(3):1046-53. PubMed ID: 1900307 [Abstract] [Full Text] [Related]
28. OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene. Chaki M, Sengupta M, Mukhopadhyay A, Subba Rao I, Majumder PP, Das M, Samanta S, Ray K. Ann Hum Genet; 2006 Sep; 70(Pt 5):623-30. PubMed ID: 16907708 [Abstract] [Full Text] [Related]
32. One-allele system in the Korean for MboI-RFLP in exon 1 of the human tyrosinase (TYR) gene. Kim DK, Kang KH, Choi IJ. J Dermatol Sci; 2000 Sep; 24(1):1-3. PubMed ID: 10960773 [Abstract] [Full Text] [Related]
33. Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism. Spritz RA, Strunk KM, Hsieh CL, Sekhon GS, Francke U. Am J Hum Genet; 1991 Feb; 48(2):318-24. PubMed ID: 1899321 [Abstract] [Full Text] [Related]
39. Cloning and sequence analysis of the tyrosinase gene from a patient with tyrosinase-positive oculocutaneous albinism. Matsunaga J, Takeda A, Tomita Y, Hara M, Shibahara S, Tagami H. J Dermatol Sci; 1992 May; 3(3):181-5. PubMed ID: 1498098 [Abstract] [Full Text] [Related]
40. R278TER and P431L mutations of the tyrosinase gene exist in Japanese patients with tyrosinase-negative oculocutaneous albinism. Matsunaga J, Dakeishi M, Shimizu H, Tomita Y. J Dermatol Sci; 1996 Nov; 13(2):134-9. PubMed ID: 8953413 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]