Correction: Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

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Correction: Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

[This corrects the article DOI: 10.1371/journal.pone.0152439.].

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Cervical spinal cord atrophy

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SMN1 and NAIP genes deletions in different types of spinal muscular atrophy in Khuzestan province, Iran

 Background: Spinal muscular atrophy (SMA) is the second most common lethal autosomal recessive disease. It is a neuromuscular disorder caused by degenerative of lower motor neurons and occasionally bulbar neurons leading to progressive limb paralysis and muscular atrophy. The SMN1 gene is recognized as a SMA causing gene while NAIP has been characterized as a modifying factor for the clinical ...

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How do SMA-linked mutations of SMN1 lead to structural/functional deficiency of the SMA protein?

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ژورنال

عنوان ژورنال: PLOS ONE

سال: 2016

ISSN: 1932-6203

DOI: 10.1371/journal.pone.0167886