U. Rüfenacht

Ancestral Founder of Mutation W283X in the Porphobilinogen Deaminase Gene among Acute Intermittent Porphyria Patients

X. Schneider-Yin, J. Deybach, E. Minder, 2002, Human Heredity.

Haplotype analysis in determination of the heredity of erythropoietic protoporphyria among Swiss families.

X. Schneider-Yin, J. Deybach, E. Minder, 2001, The Journal of investigative dermatology.

Systematic analysis of molecular defects in the ferrochelatase gene from patients with erythropoietic protoporphyria.

B. Schäfer, X. Schneider-Yin, J. Deybach, 1998, American journal of human genetics.

Influence of Age and Gender on the Clinical Expression of Acute Intermittent Porphyria Based on Molecular Study of Porphobilinogen Deaminase Gene Among Swiss Patients

X. Schneider-Yin, J. Deybach, E. Minder, 2001, Molecular medicine.

New missense mutation in the human ferrochelatase gene in a family with erythropoietic protoporphyria: functional studies and correlation of genotype and phenotype.

X. Schneider-Yin, J. Deybach, L. Gouya, 2001, Clinical chemistry.

Mutations in the ferrochelatase gene of four Spanish patients with erythropoietic protoporphyria.

X. Schneider-Yin, J. Deybach, L. Gouya, 1998, The Journal of investigative dermatology.

Mutations in the iron-sulfur cluster ligands of the human ferrochelatase lead to erythropoietic protoporphyria

M. Dorsey, X. Schneider-Yin, J. Deybach, 2000 .

Mutations in the iron-sulfur cluster ligands of the human ferrochelatase lead to erythropoietic protoporphyria.

M. Dorsey, X. Schneider-Yin, J. Deybach, 2000, Blood.