Novel guanidinoacetate methyltransferase (GAMT) mutation associated with cerebral creatine deficiency syndrome in a Syrian child: a case report. - Physician's Weekly


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Novel guanidinoacetate methyltransferase (GAMT) mutation associated with cerebral creatine deficiency syndrome in a Syrian child: a case report.

May 29, 2023

ABOUT THE CONTRIBUTORS

  • Dima Alhomsi

    Faculty of Medicine, Damascus University.

    Dania Abdalsalam

    Faculty of Medicine, Damascus University.

    Rama Sulaiman

    Faculty of Medicine, Damascus University.

    Sameer Bakleh

    Department of Neurology, Pediatrics University Hospital.

    Diana Alasmar

    Department of Inherited Metabolic Diseases, Pediatrics University Hospital, Damascus, Syria.

REFERENCES & ADDITIONAL READING

PubMed

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