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pro vyhledávání: '"M Yolanda, Raigal Martín"'
Autor:
Encarnación Pérez Pérez, José Luis Lledó Navarro, Eva Muriel Patino, M. Yolanda Raigal Martín, Miriam Moreno Prat, José María Raigal Martín
Publikováno v:
Gastroenterología y Hepatología. 31:225-228
Acute intermittent porphyria is an autosomal dominant inherited disorder resulting from a deficiency of porphobilinogen deaminase activity, the third enzyme in the heme biosynthesis pathway. This disease is uncommon, although the prevalence is higher
Autor:
M Yolanda, Raigal Martín, José Luis, Lledó Navarro, José María, Raigal Martín, Eva, Muriel Patino, Encarnación, Pérez Pérez, Miriam, Moreno Prat
Publikováno v:
Gastroenterologia y hepatologia. 31(4)
Acute intermittent porphyria is an autosomal dominant inherited disorder resulting from a deficiency of porphobilinogen deaminase activity, the third enzyme in the heme biosynthesis pathway. This disease is uncommon, although the prevalence is higher