“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2017-12-01
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| Series: | Pediatric Rheumatology Online Journal |
| Online Access: | http://link.springer.com/article/10.1186/s12969-017-0215-8 |