Takuya Takeichi
0000-0001-5958-2875
4 papers found
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Patients with keratinization disorders due to ABCA12 variants showing pityriasis rubra pilaris phenotypes
Classical Vohwinkel syndrome with heterozygous p.Asp66His mutation in GJB2 gene: Second Asian case
Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children
Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR 9C7
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