Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation

Verfasser / Beitragende:
[A. Hovnanian, A. Rochat, C. Bodemer, E. Petit, C. A. Rivers, C. Prost, S. Fraitag, A. M. Christiano, J. Uitto, M. Lathrop, Y. Barrandon, Y. de Prost]
Ort, Verlag, Jahr:
1997
Enthalten in:
American Journal of Human Genetics, 61/3(1997-09), 599-610
Format:
Artikel (online)
ID: 439477964