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28. Phenotype modifiers of spinal muscular atrophy: the number of SMN2 gene copies, deletion in the NAIP gene and probably gender influence the course of the disease. Jedrzejowska M; Milewski M; Zimowski J; Borkowska J; Kostera-Pruszczyk A; Sielska D; Jurek M; Hausmanowa-Petrusewicz I Acta Biochim Pol; 2009; 56(1):103-8. PubMed ID: 19287802 [TBL] [Abstract][Full Text] [Related]
29. The emerging role of epigenetic modifications and chromatin remodeling in spinal muscular atrophy. Lunke S; El-Osta A J Neurochem; 2009 Jun; 109(6):1557-69. PubMed ID: 19383090 [TBL] [Abstract][Full Text] [Related]
30. [Gene diagnosis for spinal muscular atrophy and its application study]. Cao DH; Ren MH; Lin CK; Cui WT; Ma HW; Wu YY; Jin CL Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):306-9. PubMed ID: 19504445 [TBL] [Abstract][Full Text] [Related]
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