Sequence Analysis of the 3′ Hypoxia-Responsive Element of the Human Erythropoietin Gene in Patients with Erythrocytosis

Author:

Percy Melanie J.,McMullin Mary Frances,Lappin Terence R.J.

Publisher

Elsevier BV

Subject

Biochemistry

Reference19 articles.

1. Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosis;de la Chapelle;Proc Natl Acad Sci,1993

2. Primary familial polycythemia: Frameshift mutation in the erythropoietin receptor gene and increased sensitivity of erythroid progenitors to erythropoietin;Sokol;Blood,1995

3. Absence of polycythemia phenotype in a child in PFCP family with Epo receptor mutation;Kralovics;Blood,1995

4. Two unique EpoR mutations associated with primary familial and congenital polycythemia;Kralovics;Blood,1995

5. Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene;Arcasoy;J Invest Med,1996

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