An adolescence-onset male leukoencephalopathy with remarkable cerebellar atrophy and novel compound heterozygous AARS2 gene mutations: a case report. [electronic resource]

By: Contributor(s): Producer: 20181012Description: 841-846 p. digitalISSN:
  • 1435-232X
Subject(s): Online resources: In: Journal of human genetics vol. 63
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Publication Type: Case Reports; Journal Article

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