Spastic paraplegia 26, autosomal recessive MeSH Supplementary Concept Data 2024

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MeSH Supplementary: Spastic paraplegia 26, autosomal recessive
Unique ID: C536862
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536862
Entry Term(s): SPG26
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Spastic paraplegia 26, autosomal recessive Preferred

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