María Dolores
Bóveda Fontán
Hospital de Cruces
Barakaldo, EspañaPublicacións en colaboración con investigadores/as de Hospital de Cruces (2)
2013
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Risk factors for developing mineral bone disease in phenylketonuric patients
Molecular Genetics and Metabolism, Vol. 108, Núm. 3, pp. 149-154
1999
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Genetic and phenotypic aspects of phenylalanine hydroxylase deficiency in Spain: Molecular survey by regions
European Journal of Human Genetics, Vol. 7, Núm. 3, pp. 386-392