Protein Identification and Haplotype Description of Homozygote Mutation Causing Congenital Plasminogen Deficiency
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Protein Identification and Haplotype Description of Homozygote Mutation Causing Congenital Plasminogen Deficiency

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Protein Identification and Haplotype Description of Homozygote Mutation Causing Congenital Plasminogen Deficiency

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Rodríguez-López, Raquel; Gimeno-Ferrer, Fátima; Esteve Martínez, Altea; Casanova-Esquembre, Andrés; Magdaleno-Tapial, Jorge; Guzmán Luján, Carola; Mena Durán, Armando V.; De Las Marinas Álvarez, María Dolores; Hernandez Bel, Laura; Hernández Bel, Pablo; Sánchez Del Pino, Manuel
This document is a artículoDate2021

    Rodríguez-López, Raquel Gimeno-Ferrer, Fátima Esteve Martínez, Altea Casanova-Esquembre, Andrés Magdaleno-Tapial, Jorge Guzmán Luján, Carola Mena Durán, Armando V. De Las Marinas Álvarez, María Dolores Hernandez Bel, Laura Hernández Bel, Pablo Sánchez Del Pino, Manuel 2021 Protein Identification and Haplotype Description of Homozygote Mutation Causing Congenital Plasminogen Deficiency Clinics In Surgery 6 3379

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