“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”

Arowolo, Afolake T; Adeola, Henry A; Khumalo, Nonhlanhla P

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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.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.uri	http://dx.doi.org/10.1186/s12969-017-0215-8
dc.identifier.uri	http://hdl.handle.net/11427/26749
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.language.iso	en
dc.publisher	BioMed Central
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
dc.date.updated	2017-12-31T04:17:11Z
dc.rights.holder	The Author(s).
dc.publisher.institution	University of Cape Town
dc.publisher.faculty	Faculty of Health Sciences	en_ZA
dc.publisher.department	Division of Dermatology	en_ZA
uct.type.filetype	Text
uct.type.filetype	Image
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.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.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