Barić I, Mardesić D, Gjurić G, Sarnavka V, Göbel-Schreiner B, Lichter-Konecki U, Konecki D S, Trefz F K
Department of Pediatrics, University Hospital Rebro, Zagreb, Croatia.
Hum Genet. 1992 Sep-Oct;90(1-2):155-7. doi: 10.1007/BF00210763.
Restriction fragment length polymorphism (RFLP) haplotypes and mutations at the phenylalanine hydroxylase (PAH) locus have been studied in 25 unrelated families from Croatia. The results of RFLP analysis demonstrated that 80% of the mutant alleles were associated with three haplotypes (1, 2 and 4). Eight mutations were detected on the background of six mutant haplotypes, comprising 68% of phenylketonuria (PKU) alleles in Croatia. The mutation in codon 408 was most frequent, as was the haplotype 2 allele with which it was associated. These data are in accordance with formerly published population genetic analyses at the PAH locus, and with studies revealing the molecular basis of the phenotypic heterogeneity of PKU. The codon 281 mutation was more frequent in Croatia than previously observed in other populations.
我们对来自克罗地亚的25个无亲缘关系的家庭进行了苯丙氨酸羟化酶(PAH)基因座的限制性片段长度多态性(RFLP)单倍型和突变研究。RFLP分析结果表明,80%的突变等位基因与三种单倍型(1、2和4)相关。在六种突变单倍型背景下检测到八个突变,占克罗地亚苯丙酮尿症(PKU)等位基因的68%。密码子408处的突变最为常见,与其相关的单倍型2等位基因也是如此。这些数据与之前发表的PAH基因座群体遗传学分析结果一致,也与揭示PKU表型异质性分子基础的研究结果一致。密码子281突变在克罗地亚比之前在其他人群中观察到的更为频繁。