Gene: STMN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3925
Gene Symbol: STMN1
STMN1 		0.030 GeneticVariation disease BEFREE A rare variant with associated myoclonic epilepsy and lower motor neuron disease had been previously described in three families before the SMN gene, responsible for the common form of SMA, was isolated. 12571787 2002
Entrez Id: 3925
Gene Symbol: STMN1
STMN1 		0.030 GeneticVariation disease BEFREE Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): a potential susceptibility factor for adult-onset lower motor neuron disease. 11993528 2002
Entrez Id: 3925
Gene Symbol: STMN1
STMN1 		0.030 GeneticVariation disease BEFREE Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease. 9585359 1998