“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”
Journal Article
2017-12-29
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Journal Title
Pediatric Rheumatology
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BioMed Central
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University of Cape Town
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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”.
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Reference:
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.