K. Ata

An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)

R. Nagel, R. Schwartz, Y. Yawata, 1992 .

An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON).

R. Nagel, R. Schwartz, Y. Yawata, 1992, Blood.

Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies.

T. Sugihara, Y. Yawata, O. Yamada, 1994, International journal of hematology.

[Concordant improvement of progressive systemic sclerosis and chronic myelogenous leukemia with interferon-alpha treatment].

T. Sugihara, Y. Yawata, O. Yamada, 1994, [Rinsho ketsueki] The Japanese journal of clinical hematology.

A Deletional Frameshift Mutation of the P-Spectrin Gene Associated With Elliptocytosis in Spectrin Tokyo ( P 220 / 216 )

Horiguchi, Y. Yawata, K. Ata, 2003 .

Molecular characterization and nonradioactive detection of beta-thalassemia in Malaysia.

S. Fucharoen, Y. Fukumaki, K. Ata, 1990, Acta haematologica.