N. Ohtsuka

Phenylketonuria mutant alleles in different populations: missense mutation in exon 7 of phenylalanine hydroxylase gene.

Y. Takarada, S. Kagawa, J. Kalanin, 1993, Clinical chemistry.

Gypsy phenylketonuria: a point mutation of the phenylalanine hydroxylase gene in Gypsy families from Slovakia.

Y. Takarada, S. Kagawa, J. Kalanin, 1994, American journal of medical genetics.

Novel mutation in exon 7 of phenylalanine hydroxylase gene in a Chinese patient with phenylketonuria.

Y. Takarada, S. Kagawa, A. Matsuoka, 1993, Clinical chemistry.

[Clinical utility of thallium-201 chloride in the diagnosis of parathyroid glands in patients with hyperparathyroidism].

K. Torizuka, M. Maki, K. Kusakabe, 1993, Kaku igaku. The Japanese journal of nuclear medicine.