| dc.contributor.author | Smith, CJ | en_US |
| dc.contributor.author | Williams, JL | en_US |
| dc.contributor.author | Hall, C | en_US |
| dc.contributor.author | Caley, MP | en_US |
| dc.contributor.author | O'Toole, EA | en_US |
| dc.contributor.author | Prasad, R | en_US |
| dc.contributor.author | Metherell, LA | en_US |
| dc.date.accessioned | 2023-03-21T11:07:31Z | |
| dc.date.issued | 2022 | en_US |
| dc.identifier.issn | 0022-202X | en_US |
| dc.identifier.uri | https://qmro.qmul.ac.uk/xmlui/handle/123456789/85104 | |
| dc.format.extent | S211 - S211 | en_US |
| dc.title | Sphingosine 1-phosphate lyase insufficiency induced ichthyosis is due to sphingolipid imbalance, increased differentiation, and aberrant intercellular junctions | en_US |
| dc.type | Conference Proceeding | |
| pubs.author-url | https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000897174500181&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6a | en_US |
| pubs.issue | 12 | en_US |
| pubs.notes | Not known | en_US |
| pubs.publication-status | Published | en_US |
| pubs.volume | 142 | en_US |
| qmul.funder | ACTH receptor pathway defects as the cause of Familial Glucocorticoid Deficiency type 3 (FGD3)::Medical Research Council | en_US |
| qmul.funder | ACTH receptor pathway defects as the cause of Familial Glucocorticoid Deficiency type 3 (FGD3)::Medical Research Council | en_US |
| qmul.funder | ACTH receptor pathway defects as the cause of Familial Glucocorticoid Deficiency type 3 (FGD3)::Medical Research Council | en_US |
| qmul.funder | ACTH receptor pathway defects as the cause of Familial Glucocorticoid Deficiency type 3 (FGD3)::Medical Research Council | en_US |
