Epidermolysis bullosa simplex: recurrent and de novo mutations in the KRT5 and KRT14 genes, phenotype/genotype correlations, and implications for genetic counseling and prenatal diagnosis (Q34560073)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Epidermolysis bullosa simplex: recurrent and de novo mutations in the KRT5 and KRT14 genes, phenotype/genotype correlations, and implications for genetic counseling and prenatal diagnosis |
scientific article |
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Epidermolysis bullosa simplex: recurrent and de novo mutations in the KRT5 and KRT14 genes, phenotype/genotype correlations, and implications for genetic counseling and prenatal diagnosis (English)
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Jouni Uitto
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Ellen G Pfendner
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Sara G Sadowski
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1 August 2005
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125
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239-243
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