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Spastic Paraplegia 44, Autosomal Recessive MeSH Supplementary Concept Data 2024


MeSH Supplementary
Spastic Paraplegia 44, Autosomal Recessive
Unique ID
C567707
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567707
Registry Number
0
Heading Mapped to
*Spastic Paraplegia, Hereditary
Frequency
0
Note
also known as SPG44; associated with mutations of GJC2 gene which encodes gap junction protein, gamma-2
Date of Entry
2012/08/24
Spastic Paraplegia 44, Autosomal Recessive Preferred
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