Pediatric Rheumatology Online Journal (Dec 2017)

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

  • Afolake T. Arowolo,
  • Henry A. Adeola,
  • Nonhlanhla P. Khumalo

DOI
https://doi.org/10.1186/s12969-017-0215-8
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 1

Abstract

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