“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”
| dc.contributor.author | Arowolo, Afolake T | |
| dc.contributor.author | Adeola, Henry A | |
| dc.contributor.author | Khumalo, Nonhlanhla P | |
| dc.date.accessioned | 2018-01-09T07:39:35Z | |
| dc.date.available | 2018-01-09T07:39:35Z | |
| dc.date.issued | 2017-12-29 | |
| dc.date.updated | 2017-12-31T04:17:11Z | |
| dc.description.abstract | A letter to the editor making some recommendations on the article entitled “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”. | |
| dc.identifier.apacitation | Arowolo, A. T., Adeola, H. A., & Khumalo, N. P. (2017). “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”. <i>Pediatric Rheumatology</i>, http://hdl.handle.net/11427/26749 | en_ZA |
| dc.identifier.chicagocitation | Arowolo, Afolake T, Henry A Adeola, and Nonhlanhla P Khumalo "“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”." <i>Pediatric Rheumatology</i> (2017) http://hdl.handle.net/11427/26749 | en_ZA |
| dc.identifier.citation | Arowolo, A. T., Adeola, H. A., & Khumalo, N. P. (2017). Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease. Pediatric Rheumatology, 15(1), 88. | |
| dc.identifier.ris | TY - AU - Arowolo, Afolake T AU - Adeola, Henry A AU - Khumalo, Nonhlanhla P AB - A letter to the editor making some recommendations on the article entitled “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”. DA - 2017-12-29 DB - OpenUCT DO - 10.1186/s12969-017-0215-8 DP - University of Cape Town J1 - Pediatric Rheumatology LK - https://open.uct.ac.za PB - University of Cape Town PY - 2017 T1 - “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” TI - “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” UR - http://hdl.handle.net/11427/26749 ER - | en_ZA |
| dc.identifier.uri | http://dx.doi.org/10.1186/s12969-017-0215-8 | |
| dc.identifier.uri | http://hdl.handle.net/11427/26749 | |
| dc.identifier.vancouvercitation | Arowolo AT, Adeola HA, Khumalo NP. “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”. Pediatric Rheumatology. 2017; http://hdl.handle.net/11427/26749. | en_ZA |
| dc.language.iso | en | |
| dc.publisher | BioMed Central | |
| dc.publisher.department | Division of Dermatology | en_ZA |
| dc.publisher.faculty | Faculty of Health Sciences | en_ZA |
| dc.publisher.institution | University of Cape Town | |
| dc.rights.holder | The Author(s). | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.source | Pediatric Rheumatology | |
| dc.source.uri | https://link.springer.com/journal/12969 | |
| dc.title | “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” | |
| dc.type | Journal Article | |
| uct.type.filetype | Text | |
| uct.type.filetype | Image |