A. Hovnanian
The Wellcome Trust Centre for Human Genetics
University of Oxford
United Kingdom
Name/email consistency: high
- Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation. Hovnanian, A., Rochat, A., Bodemer, C., Petit, E., Rivers, C.A., Prost, C., Fraitag, S., Christiano, A.M., Uitto, J., Lathrop, M., Barrandon, Y., de Prost, Y. Am. J. Hum. Genet. (1997)