Neuronal apoptosis inhibitor protein gene sequence and mutations causative of spinal muscular atrophy
US6429011B1 · kind B1 · utility
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15Claims
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Key dates
| Filing date | Jan 28, 2000 |
| Grant date | Aug 6, 2002 |
| Priority date | — |
| Expiry date | Jan 28, 2020 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12Q1/6883
- WIPO fieldMeasurement
- WIPO sectorInstruments
Abstract
The gene for autosomal recessive neurodegenerative disorder Spinal Muscular Atrophy has been mapped to a region of chromosome 5. The gene encodes a protein having homology with apoptosis inhibitor proteins of viruses so that the encoded protein has been labelled as a neuronal apoptosis inhibitor protein (NAIP). A deletion in the (NAIP) domain was identified in persons with Type I, II and III Spinal Muscular Atrophy (SMA) and not in the normal non-SMA population.
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