(Q8041562)

English

X-linked spinal muscular atrophy type 2

medical condition

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class of disease

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neurogenic arthrogryposis multiplex congenita

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genetic association

1 reference

Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy

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MeSH descriptor ID

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imported from Wikimedia project

English Wikipedia

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UniProt disease ID

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