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2. A case of recessive dystrophic epidermolysis bullosa with a novel c.6885_6898del14 mutation in the COL7A1 gene. Issue 1 (October 2017)

4. A single laminin subunit deficiency alters other laminin expression depending on the mutated genes. Issue 1 (October 2016)

5. Autoantibodies of non‐inflammatory bullous pemphigoid hardly deplete type XVII collagen of keratinocytes. Issue 12 (12th May 2017)

9. Cas9‐guided haplotyping of three truncation variants in autosomal recessive disease. Issue 7 (28th April 2022)

10. Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan. Issue 1 (18th October 2021)