Chorea due to Huntington disease-like 3 (Q86487): Difference between revisions
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Este é causado pela mutação do gene da proteína ligante TATA (SCA 17) ou raramente por herança autossômica recessiva por meio de um gene desconhecido. _x000D_ Schneider SA1, Walker RH, Bhatia KP - Síndrome de Doença de Huntington-like: o que considerar em pacientes com teste genético de Doença de Huntington negativo. | |||
| description / en | description / en | ||
This is caused by a TATA binding protein gene mutation (SCA17) or rarely autosomal recessive inherited through an unknown gene. Schneider SA1, Walker RH, Bhatia KP. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test. | |||
Revision as of 11:53, 15 August 2026
This is caused by a TATA binding protein gene mutation (SCA17) or rarely autosomal recessive inherited through an unknown gene. Schneider SA1, Walker RH, Bhatia KP. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.
| Language | Label | Description | Also known as |
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| default for all languages | ID_839962814 |
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| English | Chorea due to Huntington disease-like 3 |
This is caused by a TATA binding protein gene mutation (SCA17) or rarely autosomal recessive inherited through an unknown gene. Schneider SA1, Walker RH, Bhatia KP. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test. |
