Fingerprint
Dive into the research topics of 'GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
William A. Paznekas, Barbara Karczeski, Sascha Vermeer, R. Brian Lowry, Martin Delatycki, Faivre Laurence, Pasi A. Koivisto, Lionel Van Maldergem, Simeon A. Boyadjiev, Joann N. Bodurtha, Ethylin Wang Jabs
Research output: Contribution to journal › Review article › peer-review
188
Scopus
citations