Abstract: We report on a case of Netherton syndrome showing a new SPINK5 mutation (c.957_960dupTGGT duplication in exon 11), associated with partial defect of biotinidase.
A New SPINK5 Mutation in a Patient with Netherton Syndrome: A Case Report is a post from: Skincare
A New SPINK5 Mutation in a Patient with Netherton Syndrome: A Case Report is a post from: Skincare
A New SPINK5 Mutation in a Patient with Netherton Syndrome: A Case Report via BuzzBlazer.com
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