Gene Deletion Patterns in Spinal Muscular Atrophy Patients with Different Clinical Phenotypes

Spinal muscular atrophy (SMA) is an autosomal recessive disorder characterized by degeneration of lower motor neurons. We have assayed deletions in two candidate genes, the survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes, in 108 samples, of which 46 were from SMA p...

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Veröffentlicht in:	Journal of biomedical science 2001-03, Vol.8 (2), p.191-196
Hauptverfasser:	Haider, M.Z., Moosa, A., Dalal, H., Habib, Y., Reynold, L.
Format:	Artikel
Sprache:	eng
Schlagworte:	Original Paper
Online-Zugang:	Volltext
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