Hahn S.H.,1995
Hahn S.H., Krasnewich D., Brantly M., Kvittingen E.A., Gahl W.A. Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an american child with chronic tyrosinemia type 1. - Hum.Mut., 1995, v. 6, p. 66-73.
Hahn S.H., Krasnewich D., Brantly M., Kvittingen E.A., Gahl W.A. Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an american child with chronic tyrosinemia type 1. - Hum.Mut., 1995, v. 6, p. 66-73.
