Concepedia

Missense mutations prevalent in orientals with phenylketonuria: Molecular characterization and clinical implications

Tao Wang, Yoshiyuki Okano, Randy C. Eisensmith, Wilson H.Y. Lo, Shu‐Zhen Huang, Yi‐Tao Zeng, Lifang Yuan, Shen-Ru Liu, Savio L.C. Woo

Genomics · 1991 · 54 citations · 37 references

DOI

Concepts

References

37

Methods in Enzymology , Vol

S P Colowick, M D Joshi, Jagannathan et al. · 1966 · 26.2K citations

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A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS

Robert Guthrie, Ada Susi · PEDIATRICS · 1963 · 2.2K citations

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[32] Oligonucleotide-directed mutagenesis of DNA fragments cloned into M13 vectors

Mark J. Zoller, Michael J. Smith · Methods in enzymology on CD-ROM/Methods in enzymology · 1983 · 1.1K citations

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Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase

Simon C.M. Kwok, Fred D. Ledley, Anthony G. DiLella et al. · Biochemistry · 1985 · 323 citations

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Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria

Anthony G. DiLella, Joshua Marvit, Alan S. Lidsky et al. · Nature · 1986 · 248 citations

, , +14