Works matching DE "N-acetylglucosaminylphosphotransferase genetics"

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

Published in:

Pediatric Rheumatology, 2017, v. 15, p. 1, doi. 10.1186/s12969-017-0215-8

By:

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

Publication type:

Article