“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”
Crossref DOI link: https://doi.org/10.1186/s12969-017-0215-8
Published Online: 2017-12-29
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Arowolo, Afolake T.
Adeola, Henry A.
Khumalo, Nonhlanhla P.