Kód: 17246441
I-cell disease, or Inclusion-cell disease, is an extremely rare inherited metabolic disorder characterized by coarse facial features, skeletal afflictions and developmental delays. I-cell disease is also known as: GNPTA, Inclusion ... celý popis
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I-cell disease, or Inclusion-cell disease, is an extremely rare inherited metabolic disorder characterized by coarse facial features, skeletal afflictions and developmental delays. I-cell disease is also known as: GNPTA, Inclusion Cell Disease, Leroy Disea
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Osobní odběr Praha, Brno a 12903 dalších
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