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/s12969-017-0200-2
Published Online: 2017-09-26
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Zrhidri, Abdelali
Amasdl, Saadia
Lyahyai, Jaber
Elouardi, Hanane
Chkirate, Bouchra
Raymond, Laure
Egéa, Grégory
Taoudi, Mohamed
El Mouatassim, Said
Sefiani, Abdelaziz