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 		0.010 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