Parkinson disease synuclein gene mutation 4q21.23 (Q95966): Difference between revisions
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Doença de Parkinson autossômica dominante devida a mutação no gene da alfa-sinucleína no cromossomo 4, inicialmente descrita em uma grande família italiana e em três famílias não relacionadas de origem grega. | |||
| description / en | description / en | ||
Autosomal Dominant Parkinson Disease due to a mutation in the alpha-synuclein gene on chromosome 4 initially described in a large Italian kindred and in three unrelated families of Greek origin. | |||
Revision as of 11:48, 16 August 2026
Autosomal Dominant Parkinson Disease due to a mutation in the alpha-synuclein gene on chromosome 4 initially described in a large Italian kindred and in three unrelated families of Greek origin.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1729164793 |
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| English | Parkinson disease synuclein gene mutation 4q21.23 |
Autosomal Dominant Parkinson Disease due to a mutation in the alpha-synuclein gene on chromosome 4 initially described in a large Italian kindred and in three unrelated families of Greek origin. |
