## Communicated by Francesco Giannelli DNA sequencing revealed seven different glucose-6-phosphate dehydrogenase (G6PD) mutations in G6PD deficient subjects from 10 Polish families. Among them we found two novel mutations: 679C®T (G6PD Radlowo, class 2) and a 1006A®G (G6PD Torun, class 1). Variant
✦ LIBER ✦
Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP)
✍ Scribed by Joan Lluis Vives-Corrons; M. Assumpció Pujades; Josep Petit; Dolors Colomer; Montserrat Corbella; Josep Lluis Aguilar i Bascompte; Anna Merino
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 461 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0340-6717
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