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    Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease

    Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease by Abdelali Zrhidri, Saadia Amasdl, Jaber Lyahyai, Hanane Elouardi, Bouchra Chkirate, Laure Raymond, Grégory Egéa, Mohamed Taoudi, Said El Mouatassim, Abdelaziz Sefiani

    Published 2017
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