TRANSCENDENTAL COMMUNICATION OF TRADITIONAL CUSTODIAN IN THE KECAK RAMAYANA PERFORMING ARTS IN ULUWATU BALI




Early enzyme replacement therapy prevents dental and craniofacial abnormalities in a mouse model of mucopolysaccharidosis type VI

Mucopolysaccharidosis VI (MPS VI) is a hereditary lysosomal storage disease caused by the absence of the enzyme arylsulfatase B (ARSB).Craniofacial defects are common in MPS 7 Piece Power Reclining Sectional VI patients and manifest as abnormalities of the facial bones, teeth, and temporomandibular joints.Although enzyme replacement therapy (ERT) i

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