Publication:
Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence

dc.contributor.author Simmons, Cameron
dc.date.accessioned 2018-09-14T11:14:54Z
dc.date.available 2017-07-12T01:47:00Z
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2016-05-16 en_US
dc.date.available 2018-09-14T11:14:54Z
dc.date.issued 2016-12-01 en_US
dc.identifier.uri https://demo7.dspace.org/handle/123456789/100
dc.language English en_US
dc.title Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence en_US
dc.type Journal Article
dspace.entity.type Publication
relation.isAuthorOfPublication b1b2c768-bda1-448a-a073-fc541e8b24d9
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