Publication | Closed Access
<i>SMN1</i> gene study in three families in which ALS and spinal muscular atrophy co-exist
17
Citations
6
References
2002
Year
Neurological DisorderGeneticsGenetic EpidemiologyMolecular GeneticsDisease Gene IdentificationAls CasesNeurologyNeuropathologyMotor Neuron DiseasesRehabilitationNeuromuscular PathologyNeuromuscular DisordersNeurodegenerative DiseasesSmn1 Gene DeletionsAmyotrophic Lateral SclerosisGenetic DisorderDegenerative DiseaseSpinal Muscular AtrophyMedicine
Spinal muscular atrophy (SMA) is caused by SMN1 gene deletions or mutations, and ALS is the most frequent motor neuron condition in adults. The authors describe three families in which ALS and SMA coexist. The authors found that no SOD1 mutation was found within these families; all three ALS cases had at least two SMN1 copies; and an abnormal SMN1 gene locus did not explain the co-occurrence of these two motor neuron disorders in these families.
| Year | Citations | |
|---|---|---|
Page 1
Page 1