A splicing defect in the mouse transferrin gene leads to congenital atransferrinemia
نویسندگان
چکیده
منابع مشابه
A family of congenital atransferrinemia.
An 8-yr-old boy with familial congenital atransferrinemia was studied. He had marked hypochromic anemia but did not respond to administration of iron. The patient responded favorably to parenteral “Eisen-mangel” human serum transferrin. One gram of transferrin was infused intravenously; it disappeared almost completely from the serum within a week. However, the hemoglobin and erythrocytes incre...
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ژورنال
عنوان ژورنال: Blood
سال: 1989
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood.v74.1.482.482