A moderately frequent HindIII polymorphism at the human NGFR locus (17q12 – 17q22)
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High polymorphism at the human melanocortin 1 receptor locus.
Variation in human skin/hair pigmentation is due to varied amounts of eumelanin (brown/black melanins) and phaeomelanin (red/yellow melanins) produced by the melanocytes. The melanocortin 1 receptor (MC1R) is a regulator of eu- and phaeomelanin production in the melanocytes, and MC1R mutations causing coat color changes are known in many mammals. We have sequenced the MC1R gene in 121 individua...
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References: 1) Chung.D.W., Harris,J.E. and Davie.E.W. (1991) In Liu,C.Y. and Chien,S. (eds) Fibrinogen, Thrombosis, Coagulation and Fibrinolysis. Plenum Press, NY. pp. 39—48. 2) MUls,K.A., Buetow,K.H., Xu,Y., Weber.J.L., AJtherr,M.R., Wasmuth,J.J. and Murray,J.C. (1992) Genomics, 14, 209-219. Source/Description: The (AC)n dinucleotide repeat sequence was isolated from a human fetal retinal cDNA...
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ژورنال
عنوان ژورنال: Nucleic Acids Research
سال: 1989
ISSN: 0305-1048,1362-4962
DOI: 10.1093/nar/17.2.825