N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma
Open Access
- 1 June 1999
- journal article
- research article
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 8 (6), 971-976
- https://doi.org/10.1093/hmg/8.6.971