Severe Neutropenia in Japanese Patients with X-Linked Agammaglobulinemia

Author:

Kanegane Hirokazu,Taneichi Hiromichi,Nomura Keiko,Futatani Takeshi,Miyawaki Toshio

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Reference24 articles.

1. Stiehm ER, Ochs HD, Winkelstein JA: Immunodeficiency disorders: General consideration. In Immunologic disorders in infants and children, ER Stiehm, HD Ochs, JA Winkelstein (eds). Philadelphia, WB Saunders, 2004, pp. 289–355

2. Conley ME, Howard V: Clinical findings leading to the diagnosis of X-linked agammaglobulinemia. J Pediatr 141:566–571, 2002

3. Kornfeld SJ, Good RA, Litman GW: Atypical X-linked agammaglobulinemia. N Engl J Med 331: 949–951, 1994

4. Kornfled SJ, Haire RN, Strong SJ, Tang H, Sung SS, Fu SM, Litman GW: A novel mutation (Cys145 → Stop) in Bruton’s tyrosine kinase is associated with newly diagnosed X-linked agammaglobulinemia in a 51-year-old male. Mol Med 2:619–623, 1996

5. Bykowsky MJ, Haire RN, Ohta Y, Tang H, Sung SS, Veksler ES, Green JM, Fu SM, Litman GW, Sullivan KE: Discordant phenotype in siblings with X-linked agammaglobulinemia. Am J Hum Genet 58:477–483, 1996

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