| molybdenum cofactor d. |
an autosomal recessive disorder in which deficiency of the molybdenum cofactor causes deficiency of the molybdoenzymes sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase, resulting in severe neurologic abnormalities, dislocated ocular lenses, mental retardation, xanthinuria, and early death.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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