SPG61 |
SPGF |
chromosome 3 open reading frame 13 |
||
[Spastic paraplegia 64] This designation has been used in some databanks to refer to the gene encoding one particular form of autosomal recessive spastic paraplegia, a neurodegenerative motor neuron disease characterized by progressive age-dependent loss of corticospinal motor tract function. SPG64 is the result of mutations in the ENTPD1 [ectonucleoside triphosphate diphosphohydrolase 1] (see also: CD39) (Novarino et al, 2014).
For additional information on CD antigens see also: CD antigens Dictionary.
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