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Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome

✍ Scribed by Corinne Vasseur-Godbillon; Michael C. Marden; Piero Giordano; Henri Wajcman; Véronique Baudin-Creuza


Book ID
116304188
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
277 KB
Volume
37
Category
Article
ISSN
1079-9796

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