Additional file 2. Table S1. Clinical features and detected mutated genes and variants of the 26 confirmed PCD patients of Chinese origin. a. The patients are listed according to different categories
Spinal muscular atrophy (SMA) is a common genetic motor neuron (MN) disease caused by low levels of the ubiquitously expressed housekeeping survival motor neuron (SMN) protein, whereas concomitant ove
Raw data obtained by Real time PCR performed to assess the expression of muscle-specific miRNAs, miR206, miR-133a, miR-133b, miR-1, in serum of 21 infantile SMA patients at baseline and after 6 months
