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Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients

โœ Scribed by Asako Nakamura; Shinya Matsuura; Hiroshi Tauchi; Ryoji Hanada; Hirofumi Ohashi; Tomonobu Hasegawa; Koujiro Honda; Mitsuo Masuno; Kiyoshi Imaizumi; Katsuo Sugita; Toshinori Ide; K. Komatsu


Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
127 KB
Volume
44
Category
Article
ISSN
1435-232X

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Fanconi anemia (FA), an autosomal recessive disorder characterized by a progressive pancytopenia associated with congenital anomalies and high predisposition to malignancies, is a genetically and clinically heterogeneous disease. At least eight complementation groups (FA-A to FA-H) have been identif