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Functional and splicing defect analysis of 23 ACVRL1 mutati..:
Alaa el Din, Ferdos
;
Patri, Sylvie
;
Thoreau, Vincent
...
PLOS ONE. 10 (2015) 7 - p. e0132111 , 2015
Link:
https://doi.org/10.1371/journal.pone.0132111
RT Journal T1
Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1371_journal.pone.0132111&Exemplar=1&LAN=DE A1 Alaa el Din, Ferdos A1 Patri, Sylvie A1 Thoreau, Vincent A1 Rodriguez-Ballesteros, Montserrat A1 Hamade, Eva A1 Bailly, Sabine A1 Gilbert-Dussardier, Brigitte A1 Abou Merhi, Raghida A1 Kitzis, Alain A1 Buratti, Emanuele PB Public Library of Science (PLoS) YR 2015 SN 1932-6203 JF PLOS ONE VO 10 IS 7 SP e0132111 LK http://dx.doi.org/https://doi.org/10.1371/journal.pone.0132111 DO https://doi.org/10.1371/journal.pone.0132111 SF ELIB - SuUB Bremen
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