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Comorbid genetic diseases, von Hippel-Lindau disease and spinocerebellar ataxia type 2, confounding the diagnosis of cerebellar dysfunction in an adolescent

✍ Scribed by D.Elizabeth McNeil; W.Marston Linehan; Gladys M Glenn


Book ID
119532379
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
98 KB
Volume
103
Category
Article
ISSN
0303-8467

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