Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes in spinal muscular atrophy (SMA) patients in Malaysia [RJ482.A83 W333 2008 f rb].

Mohd Shamshudin, Wati @ Hayati (2007) Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes in spinal muscular atrophy (SMA) patients in Malaysia [RJ482.A83 W333 2008 f rb]. Masters thesis, Universiti Sains Malaysia.

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Abstract

Spinal Muscular Atrophy (SMA) adalah sejenis penyakit kelemahan saraf otot yang akhirnya menyebabkan kemerosotan otot. Penyakit ini disebabkan oleh mutasi pada gen Survival Motor Neuron 1 (SMN1). Spinal Muscular Atrophy (SMA) is a neuromuscular disease which is clinically characterized by progressive muscular weakness and atrophy of the skeletal muscles.

Item Type: Thesis (Masters)
Subjects: R Medicine > RJ Pediatrics > RJ370-550 Diseases of children and adolescents
Divisions: Kampus Kesihatan (Health Campus) > Pusat Pengajian Sains Perubatan (School of Medical Sciences) > Thesis
Depositing User: Mr Erwan Roslan
Date Deposited: 14 May 2009 01:39
Last Modified: 15 May 2017 04:43
URI: http://eprints.usm.my/id/eprint/10002

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