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Dive into the research topics of 'G59A mutation in the GJB2 gene in a Taiwanese family with knuckle pads, palmoplantar keratoderma and sensorineural hearing loss'. Together they form a unique fingerprint.- Sort by
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L. H. Chen, H. C. Lin, H. M. Sheu, S. C. Chao
Research output: Contribution to journal › Letter › peer-review