AAAAAA

   
Results: 1-5 |
Results: 5

Authors: GOUYA L SCHNEIDERYIN X RUFENACHT U HERRERO C LECHA M MASCARO JM PUY H DEYBACH JC MINDER EI
Citation: L. Gouya et al., MUTATIONS IN THE FERROCHELATASE GENE OF 4 SPANISH PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA, Journal of investigative dermatology, 111(3), 1998, pp. 406-409

Authors: RUFENACHT UB GOUYA L SCHNEIDERYIN X PUY H SCHAFER BW AQUARON R NORDMANN Y MINDER EI DEYBACH JC
Citation: Ub. Rufenacht et al., SYSTEMATIC ANALYSIS OF MOLECULAR DEFECTS IN THE FERROCHELATASE GENE FROM PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA, American journal of human genetics, 62(6), 1998, pp. 1341-1352

Authors: MINDER EI SCHNEIDERYIN X
Citation: Ei. Minder et X. Schneideryin, AGE-DEPENDENT REFERENCE VALUES OF URINARY PORPHYRINS IN CHILDREN, European journal of clinical chemistry and clinical biochemistry, 34(5), 1996, pp. 439-443

Authors: SCHNEIDERYIN X SCHAFER BW TONZ O MINDER EI
Citation: X. Schneideryin et al., HUMAN FERROCHELATASE - A NOVEL MUTATION IN PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA AND AN ISOFORM CAUSED BY ALTERNATIVE SPLICING, Human genetics, 95(4), 1995, pp. 391-396

Authors: SCHNEIDERYIN X TAKETANI S SCHAFER B MINDER EI
Citation: X. Schneideryin et al., RECESSIVE INHERITANCE OF ERYTHROPOIETIC PROTOPORPHYRIA WITH LIVER-FAILURE, Lancet, 344(8918), 1994, pp. 337-337
Risultati: 1-5 |