PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

Author:

Imashuku Shinsaku,Muramatsu Hideki,Sugihara Takashi,Okuno Yusuke,Wang Xinan,Yoshida Kenichi,Kato Ayako,Kato Koichi,Tatsumi Yasuaki,Hattori Ai,Kita Shinya,Oe Keishi,Sueyoshi Atsushi,Usui Takeshi,Shiraishi Yuichi,Chiba Kenichi,Tanaka Hiroko,Miyano Satoru,Ogawa Seishi,Kojima Seiji,Kanno Hitoshi

Funder

“Research on Measures for Intractable Diseases” Project from Ministry of Health Labour and Welfare, Grant-in-Aids from the Ministry of Health, Labor and Welfare of Japan

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Reference19 articles.

1. Jaffe ER, Gottfried EL. Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes. J Clin lnvest. 1968;47:1375–88.

2. Inoue J, Nomura M, Akagi E, Yawata Y. The Japanese family of congenital high red cell membrane phosphatidylcholine hemolytic anemia. Rinsho Ketsueki. 1989;30(11):2014–19 (article in Japanese).

3. Yawata Y. Characteristics of red cell membrane disorders in the Japanese population. Rinsho Byori. 1997;45(4):367–76 (article in Japanese).

4. Archer NM, Shmukler BE, Andolfo I, et al. Hereditary xerocytosis revisited. Am J Hematol. 2014;89(12):1142–6.

5. Clark MR, Shohet SB, Gottfried EL. Hereditary hemolytic disease with increased red blood cell phosphatidylcholine and dehydration: one, two, or many disorders? Am J Hematol. 1993;42(1):25–30.

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