Deficiency in hepatic tyrosine aminotransferase (TAT) causes tyrosinemia type II, an autosomal recessively inherited disorder. Using a TAT cosmid clone, we have identified an MspI restriction fragment length polymorphism (RFLP) 5' to the TAT gene, with allele frequencies of 0.63 and 0.37. Analysis o
โฆ LIBER โฆ
A common restriction fragment length polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidaemia
โ Scribed by E. C. Klasen; P. J. Talmud; L. Havekes; E. Wit; E. Kooij-Meijs; M. Smit; G. Hansson; S. E. Humphries
- Publisher
- Springer
- Year
- 1987
- Tongue
- English
- Weight
- 632 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0340-6717
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KEY WORDS: HTLV-I subtypes; env gene; sub-The major type of human T-lymphotropic virus type-specific nucleotides type I (HTLV-I), generally referred to as the cosmopolitan type, has been grouped into three subtypes (A, B, and C) by phylogenetic analysis of the long terminal repeat sequences of the v