| Predicate | Object |
|---|---|
| rdf:type | |
| entrezgene:geneRifText |
Homozygous GJA1 point mutations in a conserver codon, one base change results in a Oculodentodigital dysplasia phenotype in one patient, another base change in the same codon resultes in a Hallermann-Streiff syndrome phenotype in another patient.
|