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The spectrum of mutations in erythrokeratodermias – novel and de novo mutations in GJB3.
- Published in:
- Human Genetics, 2000, v. 106, n. 3, p. 321, doi. 10.1007/s004390051045
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Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis.
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- Nature Genetics, 1998, v. 20, n. 4, p. 366, doi. 10.1038/3840
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- Publication type:
- Article