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Significats de microvillus inclusion disease en anglès

rus
микроворсинчатая атрофия

Human disease.

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      микроворсинчатая атрофия
      Ús de microvillus inclusion disease en anglès
      1
      Methods: Clinical data of an infant affected with microvillus inclusion disease was collected.
      Pubmed
      2
      Conclusion: Based on the clinical and molecular evidence, the patient was diagnosed with microvillus inclusion disease.
      Pubmed
      3
      Objective: To explore the clinical features and mutations of MYO5B gene in a family affected with microvillus inclusion disease.
      Pubmed
      Translations for microvillus inclusion disease