The Neurologist: Clinical & Therapeutics Journal
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Sohail S
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Genetics of Spinal Muscular Atrophy and Splicing of Smn Gene
Spinal muscular atrophy is characterized by loss of motor neurons and muscle atrophy, largely in childhood. It is a devastating neuromuscular disorder. In humans, nearly two identical inverted SMN genes (SMN1, SMN2) are present on chromosome 5q13. Homologous deletion of SMN1 results in SMA.SMA is initiated by low levels of the survival motor neuron... Read More»
Ashraf A, Nazir S, Murtaza M, Imtiaz MU, Sohail S, Nisar M, Abbas S, Farooq M, Sohail F and Rana H
: Neurol Clin Therapeut J 6: 111
10.4172/nctj.1000110Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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