Mitochondrial Dna Depletion Syndrome 19 (MTDPS19)

Alias:
Mtdps19
Mitochondrial Dna Depletion Syndrome, Type 19
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Dna Depletion Syndrome 19, is also known as mtdps19. An important gene associated with Mitochondrial Dna Depletion Syndrome 19 is SLC25A10 (Solute Carrier Family 25 Member 10). Affiliated tissues include skeletal muscle and testis, and related phenotypes are spasticity and hearing impairment
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
4
1

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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