Published in
Elsevier, European Journal of Paediatric Neurology, 3(14), p. 253-260, 2010
DOI: 10.1016/j.ejpn.2009.09.008
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A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency
Journal article published in 2010 by
Maciej Pronicki,
Paweł Kowalski,
Dorota Piekutowska-Abramczuk,
Joanna Taybert,
Agnieszka Karkucinska-Wieckowska,
Tamara Szymanska-Debinska,
Elzbieta Karczmarewicz,
Magdalena Pajdowska,
Marek Migdal,
Bogumila Milewska-Bobula,
Jolanta Sykut-Cegielska 
,
Ewa Popowska
,
Ewa Popowska
This paper was not found in any repository, but could be made available legally by the author.
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