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Filter by author:

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Publication 12/01/1983

Human adenine phosphoribosyltransferase: characterization from subjects with a deficiency of enzyme activity.

O'Toole TE, Wilson JM, Gault MH, Kelley WN

Biochemical Genetics

Publication 9/01/1983

Human hypoxanthine-guanine phosphoribosyltransferase. Detection of a mutant allele by restriction endonuclease analysis.

Wilson JM, Frossard P, Nussbaum RL, Caskey CT, Kelley WN

The Journal Of Clinical Investigation

Publication 8/01/1983

Adenosine deaminase deficiency with normal immune function. An acidic enzyme mutation.

Daddona PE, Mitchell BS, Meuwissen HJ, Davidson BL, Wilson JM, Koller CA

The Journal Of Clinical Investigation

Publication 5/25/1983

A possible nucleotide-binding domain in the tertiary fold of phosphoribosyltransferases.

Argos P, Hanei M, Wilson JM, Kelley WN

The Journal Of Biological Chemistry

Publication 5/01/1983

Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome.

Wilson JM, Kelley WN

The Journal Of Clinical Investigation

Publication 2/01/1983

Human hypoxanthine (guanine) phosphoribosyltransferase: an amino acid substitution in a mutant form of the enzyme isolated from a patient with gout.

Wilson JM, Tarr GE, Kelley WN

Proceedings Of The National Academy Of Sciences Of The United States Of America