| Translated title of the contribution | Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of congenital eye malformations |
|---|---|
| Original language | English |
| Pages (from-to) | 165 - 172 |
| Journal | Human Molecular Genetics |
| Volume | 8 |
| Publication status | Published - 1999 |
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