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Description
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As in PraderWillis syndrome, individuals with Angelmans syndrome who have typical OCA2 features have been described.62 Mutations in the TYRP1 gene result in OCA3 (OMIM #203290)

The diagnosis of the MMNST mainly relies on imaging examinations and a pathological biopsy [3]

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Arginase downregulates NO production by competing with NOS for arginine (MacMicking et al., 1997)

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