Search Results - Bouchra Chkirate

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

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Heterozygous MEFV Mutation Leading to Renal Failure: A Case Study by Souhaila El Gazzane MD, Amine Ichane MD, Chaimae Nahi MD, Khadija Mouaddine MD, Bouchra Chkirate MD, PhD, Aziza Guennoun MD, Najat Oulahiane MD, Hassan Ait Ouamar MD, PhD, Lamiaa Rouas MD, PhD

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