Spastic Paraplegia 7, Autosomal Recessive MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Spastic Paraplegia 7, Autosomal Recessive
Unique ID: C564599
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564599
Registry Number: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 2
Note: mutation in the paraplegin gene, SPG7
Date of Entry: 2012/11/05

Spastic Paraplegia 7, Autosomal Recessive Preferred

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