APA

Marchi R., Brennan S., Meyer M., Rojas H., Kanzler D., De Agrela M. & Ruiz-Saez A. (20130723). A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia. : Blood cells, molecules & diseases.

Chicago

Marchi Rita, Brennan Stephen, Meyer Michael, Rojas Héctor, Kanzler Daniela, De Agrela Marisela and Ruiz-Saez Arlette. 20130723. A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia. : Blood cells, molecules & diseases.

Harvard

Marchi R., Brennan S., Meyer M., Rojas H., Kanzler D., De Agrela M. and Ruiz-Saez A. (20130723). A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia. : Blood cells, molecules & diseases.

MLA

Marchi Rita, Brennan Stephen, Meyer Michael, Rojas Héctor, Kanzler Daniela, De Agrela Marisela and Ruiz-Saez Arlette. A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia. : Blood cells, molecules & diseases. 20130723.