L. Cohen-Solal

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

G. Mollet, C. Antignac, C. Antignac, 1998, American journal of human genetics.

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

G. Mollet, C. Antignac, C. Antignac, 2001, Journal of the American Society of Nephrology : JASN.

Benign familial hematuria associated with a novel COL4A4 mutation

C. Antignac, S. Ozen, D. Ertoy, 2001, Pediatric Nephrology.

GENETIC RENAL DISEASE / ORIGINAL AR T ICLE

C. Antignac, S. Ozen, D. Ertoy, 2001 .

Diffuse esophageal leiomyomatosis with perirectal involvement mimicking Hirschsprung disease.

C. Antignac, J. Triboulet, L. Heidet, 2001, Gastroenterology.

Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical region.

C. Antignac, C. Antignac, M. Gubler, 1997, Cytogenetics and cell genetics.