Zobrazeno 1 - 1
of 1
pro vyhledávání: '"C. A. Wijngaarde"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-10 (2017)
Abstract Background Hereditary proximal spinal muscular atrophy (SMA) is a severe neuromuscular disease of childhood caused by homozygous loss of function of the survival motor neuron (SMN) 1 gene. The presence of a second, nearly identical SMN gene
Externí odkaz:
https://doaj.org/article/8c70df5be7ba4814b7799e91771fa9d1
