An ~140-kb deletion associated with feline spinal muscular atrophy implies an essential LIX1 function for motor neuron survival

The leading genetic cause of infant mortality is spinal muscular atrophy (SMA), a clinically and genetically heterogeneous group of disorders. Previously we described a domestic cat model of autosomal recessive, juvenile-onset SMA similar to human SMA type III. Here we report results of a whole-geno...

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Veröffentlicht in:	Genome Research 2006-09, Vol.16 (9), p.1084-1090
Hauptverfasser:	Fyfe, John C., Menotti-Raymond, Marilyn, David, Victor A., Brichta, Lars, Schäffer, Alejandro A., Agarwala, Richa, Murphy, William J., Wedemeyer, William J., Gregory, Brittany L., Buzzell, Bethany G., Drummond, Meghan C., Wirth, Brunhilde, O'Brien, Stephen J.
Format:	Artikel
Sprache:	eng
Schlagworte:	Letter
Online-Zugang:	Volltext
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