Severe Homozygous Protein C Deficiency: Identification of a Splice Site Missense Mutation (184, Q → H) in Exon 7 of the Protein C Gene
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X. Estivill | J. Fontcuberta | J. Soria | N. Sala | J. Barceló | L. Botero | J. Maldonado | D. Brito | Xavier Estivill | José Manuel Soria