We describe a case of spherocytosis in a French child splenectomized at age 10 years. The parents were devoid of any clinical, hematological, or biochemical abnormalities. Following splenectomy, the proposita exhibited a reduction of red cell membrane ankyrin. The variable number of dinucleotide rep
✦ LIBER ✦
High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis
✍ Scribed by Emanuele Miraglia del Giudice; Matteo Francese; Bruno Nobili; Laurette Morlé; Stefano Cutillo; Jean Delaunay; Silverio Perrotta
- Book ID
- 117166420
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 274 KB
- Volume
- 132
- Category
- Article
- ISSN
- 1097-6833
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