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A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia

✍ Scribed by Marchi, Rita; Brennan, Stephen; Meyer, Michael; Rojas, Héctor; Kanzler, Daniela; De Agrela, Marisela; Ruiz-Saez, Arlette


Book ID
123470507
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
973 KB
Volume
50
Category
Article
ISSN
1079-9796

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