A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.
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H. Huopio | J. Kere | F. Ashcroft | J. Chapman | J. Komulainen | T. Otonkoski | G. Cote | C. Ammälä | R. Ashfield | K. Cosgrove | M. Dunne | K. Cosgrove | P. Thomas | E. Huang | Juha Kere | Frances M. Ashcroft | Jorma Komulainen | Carina Ämmälä | Timo Otonkoski | Gilbert J. Cote | Gilbert J. Cote | Joanna C. Chapman | Rebecca Ashfield | Eileen Huang | Pamela M. Thomas | Frances M Ashcroft