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- W2000722435 abstract "stem. The cerebellar white matter usually has a mildly abnormal signal intensity without swelling. The clini- cal picture is characterized by macrocephaly within the first year of life. There is a delayed onset of motor dete- rioration, dominated by cerebellar ataxia. The disease has an autosomal recessive mode of inheritance. Our genetic linkage study resulted in the identification of a gene for the disease: MLC1 4" @default.
- W2000722435 created "2016-06-24" @default.
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- W2000722435 date "2009-09-01" @default.
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- W2000722435 title "MR Definition of Novel White Matter Disorders" @default.
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- W2000722435 doi "https://doi.org/10.1177/19714009090220s112" @default.
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