Abdelali Zrhidri, Saadia Amasdl, Jaber Lyahyai, Hanane Elouardi, Bouchra Chkirate, Laure Raymond, . . . Abdelaziz Sefiani. (2017). Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease. BMC.
Chicago Style (17th ed.) CitationAbdelali Zrhidri, et al. Next Generation Sequencing Identifies Mutations in GNPTG Gene as a Cause of Familial Form of Scleroderma-like Disease. BMC, 2017.
MLA (9th ed.) CitationAbdelali Zrhidri, et al. Next Generation Sequencing Identifies Mutations in GNPTG Gene as a Cause of Familial Form of Scleroderma-like Disease. BMC, 2017.
Warning: These citations may not always be 100% accurate.