Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Scherpf, S."'
Autor:
Koenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Müller, C. R., Lindlöf, M., Kaariainen, H., La Chapelle, A., Kiuru, A., Savontaus, M. -L, Gilgenkrantz, H., Récan, D., Chelly, J., Kaplan, J. -C, Angela Elvira Covone, Archidiacono, N., Romeo, G., Liechti-Gailati, S., Schneider, V., Braga, S., Moser, H., Darras, B. T., Murphy, R., Francke, U., Chen, J. D., Morgan, G., Denton, M., Greenberg, C. R., Wrogemann, K., Blonden, L. A. J., Paassen, H. M. B., Ommen, G. J. B., Kunkel, L. M.
Publikováno v:
Scopus-Elsevier
About 60% of both Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) is due to deletions of the dystrophin gene. For cases with a deletion mutation, the “reading frame” hypothesis predicts that BMD patients produce a semifuncti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9c1399124e0babfff3a37912cb22fbb2
https://pubmed.ncbi.nlm.nih.gov/2491009
https://pubmed.ncbi.nlm.nih.gov/2491009
Autor:
Koening, M., Alan Beggs, Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Muller, C. R., Lindlof, M., Kaariainen, H., La Chapelle, A., Kiuru, A., Savontaus, M. -L, Gilgenkrantz, H., Recan, D., Chelly, J., Kaplan, J. -C, Covone, A. E., Archidiacono, N.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3fe4dd9262c3ec6557a79fb48e327338
http://www.scopus.com/inward/record.url?eid=2-s2.0-0024466501&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0024466501&partnerID=MN8TOARS
