Papers: 10.1002/mgg3.1238

https://doi.org/10.1002/mgg3.1238

Spinal muscular atrophy caused by a novel <i>Alu</i> ‐mediated deletion of exons 2a‐5 in <i>SMN1</i> undetectable with routine genetic testing

Cited by: 6
Author(s): Ivana Jedličková, Anna Přistoupilová, Lenka Nosková, Filip Majer, Viktor Stránecký, Hana Hartmannová, Kateřina Hodaňová, Helena Trešlová, Michaela Hýblová, Peter Solár, Gabriel Minárik, Mária Giertlová, Stanislav Kmoch
Published: over 6 years ago

Software Mentions 1