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In cases of NAION caused by a medication, questions may arise about whether patients were sufficiently informed of this rare but serious risk
However, current clinical evidence does not support this transition
Publisher | Google Scholor Kallassy J, Gagnon E, Rosenberg D, Silbart LK, McManus SA
Our patents might not contain claims that are sufficiently broad to prevent others from utilizing our technologies
La forma ms frecuente, 80% de los casos de defecto de la N-glicosilacin, es el CDG Ia, por defecto de la enzima fosfomanomutasa 2 (PMM2) , debido a mutaciones en el gen PMM2 (cromosoma 16 p13)
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