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Massive acute haemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient preterm triplets

โœ Scribed by Varsha A Shah; Cheo Lian Yeo


Book ID
108955233
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
56 KB
Volume
43
Category
Article
ISSN
1034-4810

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โœ Ewa Jablonska-Skwiecinska; Irmina Lewandowska; Danuta Plochocka; Jacek Topczewsk ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 518 KB

## 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: 679CยฎT (G6PD Radlowo, class 2) and a 1006AยฎG (G6PD Torun, class 1). Variant