Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.
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A. Munnich | S. Lyonnet | J. Frézal | C. Caillaud | M. Berthelon | J. Rey | F. Rey | Arnold Munnich | Jean Frézal | Catherine Caillaud | F. Rey | J. Rey