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Mutation of SBDS and SH2D1A is not associated with aplastic anemia in Japanese children

Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan

Correspondence: Seiji Kojima, MD, PhD, Department Pediatrics, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550. Phone: international +81.52. 7442994. Fax: international +81.85.7442994. E-mail: kojimas{at}med.nagoya-u.ac.jp

During the last decade, the genetic basis of inherited bone marrow failure syndromes has been identified. Recently, genetic factors predisposing to aplastic anemia (AA) have been found in a few patients with apparently acquired AA. Here we present the genetic analysis of SBDS and SH2D1A in Japanese children with AA.

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				H. Yamaguchi, J. Takeuchi, H. Tamai, Y. Mitamura, F. Kosaka, K. Dan, and K. Inokuchi Identification of the SBDS Gene Mutation in Japanese Patients with Bone Marrow Failure Syndrome Blood (ASH Annual Meeting Abstracts), November 16, 2008; 112(11): 4117 - 4117. [Abstract]