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Author/Creator Swoboda, K

1. Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy. Issue 2 (2nd February 2005)

Authors:
Lampe, A K; Dunn, D M; von Niederhausern, A C; Hamil, C; Aoyagi, A; Laval, S H; Marie, S K; Chu, M-L; Swoboda, K; Muntoni, F; Bonnemann, C G; Flanigan, K M; Bushby, K M D; Weiss, R B
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 2(2005)
Page Start:
108
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. P.065 AVXS-101 gene-replacement therapy (GRT)) in presymptomatic spinal muscular atrophy (SMA): study update. (5th June 2019)

Authors:
Schultz, M; Swoboda, K; Farrar, M; McMillan, H; Parsons, J; Farrow, M; Ogrinc, FG; Feltner, DE; McGill, BE; Spector, SA; L'Italien, J; Sproule, DM; Strauss, KA
Journal:
Canadian journal of neurological sciences
Issue:
Volume 46(2019)Supplement 1
Page Start:
S31
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. P.065 AVXS-101 gene-replacement therapy (GRT)) in presymptomatic spinal muscular atrophy (SMA): study update. (June 2019)

Authors:
Schultz, M; Swoboda, K; Farrar, M; McMillan, H; Parsons, J; Farrow, M; Ogrinc, FG; Feltner, DE; McGill, BE; Spector, SA; L'Italien, J; Sproule, DM; Strauss, KA
Journal:
Canadian journal of neurological sciences
Issue:
Volume 46(2019)Supplement 1
Page Start:
S31
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗