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Neu–Laxova Syndrome Neu–Laxova syndrome, first described in 1971, is clinically associated with microcephaly, anomalies of the limbs, atrophic gyri, and absence of the corpus callosum, along with atrophy of the cerebrum, cerebellum, and pons (84)
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Crystal structure of maleylacetoacetate isomerase/glutathione transferase zeta reveals the molecular basis for its remarkable catalytic promiscuity
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