| 1. | Mutations in this gene are associated with autosomal recessive spastic paraplegia-15.
|
| 2. | This is the case in Friedreich's ataxia, hereditary spastic paraplegia, and Wilson's disease.
|
| 3. | The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia.
|
| 4. | Dysfunction of PI4K2A may contribute to tumour growth, spastic paraplegia, Gaucher's disease, or Alzheimer's disease.
|
| 5. | Together with French physician Maurice Lorrain, the eponymous Str�mpell Lorrain disease is named, which is an hereditary spastic paraplegia.
|
| 6. | Additionally the loss of its production appears to be one cause of the human neurological disease, Hereditary spastic paraplegia.
|
| 7. | Those include genes linked to early onset Alzheimer's, spastic paraplegia, NiemannPick disease and a severe form of Usher syndrome.
|
| 8. | This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders as well as spastic ataxia-neuropathy syndrome.
|
| 9. | Mutations in the SPG21 ( ACP33 / maspardin ) gene are associated with the mast syndrome, a type of spastic paraplegia.
|
| 10. | Mutations in the " ATL1 " gene are also a common cause of early-onset hereditary spastic paraplegia ( HSP ) in humans.
|
मोबाइल