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Published in 2019 at "Human gene therapy"
DOI: 10.1089/hum.2019.049
Abstract: Netherton Syndrome (NS) is a rare autosomal recessive skin disorder caused by mutations in SPINK5. It is a debilitating condition with notable mortality in the early years of life. There is no curative treatment. We…
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Keywords:
gene modified;
application gene;
netherton syndrome;
epidermal sheets ... See more keywords