Amyotrophic lateral sclerosis type 15
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Sign InDescription
Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene.
Mode of Inheritance
- X-linked dominant inheritance
VARIANTS
35
Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene.
VARIANTS
35