Genetic heterogeneity of neuronal intranuclear inclusion disease: What about the infantile variant?
Genetic heterogeneity of neuronal intranuclear inclusion disease: What about the infantile variant?
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United States: John Wiley & Sons, Inc
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Language
English
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Publisher
United States: John Wiley & Sons, Inc
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(1985) F // North American Indian// unaffected nonconsaguineous parents born 1 mth premature (2.2 kg) // developed normal, but free walked at 1.5 yrs; speech delay; poor articulation 3.5 yrs // unsteady gait (frequent falls), hypotonia, areflexia, scoliosis, delayed behavioral development, microcephaly (−2SD) seizures, ataxia, nystagmus, choreoathe...
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Full title
Genetic heterogeneity of neuronal intranuclear inclusion disease: What about the infantile variant?
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TN_cdi_doaj_primary_oai_doaj_org_article_dea1084fd49445ff946d063b7ee1ca59
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_dea1084fd49445ff946d063b7ee1ca59
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ISSN
2328-9503
E-ISSN
2328-9503
DOI
10.1002/acn3.51332
