Autosomal Recessive Spastic Paraplegia Type 59 (SPG59)

Alias:
Spg59
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Recessive Spastic Paraplegia Type 59, is also known as spg59. An important gene associated with Autosomal Recessive Spastic Paraplegia Type 59 is USP8 (Ubiquitin Specific Peptidase 8). Affiliated tissues include cerebellum, and related phenotypes are spastic paraplegia and clonus
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Infant
<1/1000000
1
4
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
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