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bn:00663962n
Noun Concept
JA
No term available
EN
VLDLR-associated cerebellar hypoplasia is a rare autosomal recessive condition caused by a disruption of the VLDLR gene. Wikipedia
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IS A
希少疾患
症候群
EN
autosomal recessive disease
EN
autosomal recessive cerebellar ataxia
GENETIC ASSOCIATION
EN
CA8
EN
VLDL receptor

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