Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Evan Gale"'
Autor:
John F Staropoli, Larissa Haliw, Sunita Biswas, Lillian Garrett, Sabine M Hölter, Lore Becker, Sergej Skosyrski, Patricia Da Silva-Buttkus, Julia Calzada-Wack, Frauke Neff, Birgit Rathkolb, Jan Rozman, Anja Schrewe, Thure Adler, Oliver Puk, Minxuan Sun, Jack Favor, Ildikó Racz, Raffi Bekeredjian, Dirk H Busch, Jochen Graw, Martin Klingenspor, Thomas Klopstock, Eckhard Wolf, Wolfgang Wurst, Andreas Zimmer, Edith Lopez, Hayat Harati, Eric Hill, Daniela S Krause, Jolene Guide, Ella Dragileva, Evan Gale, Vanessa C Wheeler, Rose-Mary Boustany, Diane E Brown, Sylvie Breton, Klaus Ruether, Valérie Gailus-Durner, Helmut Fuchs, Martin Hrabě de Angelis, Susan L Cotman
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e38310 (2012)
Cln3(Δex7/8) mice harbor the most common genetic defect causing juvenile neuronal ceroid lipofuscinosis (JNCL), an autosomal recessive disease involving seizures, visual, motor and cognitive decline, and premature death. Here, to more thoroughly inv
Externí odkaz:
https://doaj.org/article/1d1ada78800e44e893b4656b106c2943
Autor:
Rose-Mary Boustany, Dirk H. Busch, Daniela S. Krause, Sergej Skosyrski, Evan Gale, Raffi Bekeredjian, Julia Calzada-Wack, Lillian Garrett, Eckhard Wolf, Anja Schrewe, Susan L. Cotman, Birgit Rathkolb, Sabine M. Hölter, John F. Staropoli, Frauke Neff, Lore Becker, Eric Hill, Vanessa C. Wheeler, Sunita Biswas, Andreas Zimmer, Hayat Harati, Jack Favor, Edith Lopez, Sylvie Breton, Jan Rozman, Oliver Puk, Jolene R. Guide, Minxuan Sun, Patricia da Silva-Buttkus, Helmut Fuchs, Thomas Klopstock, Diane E. Brown, Valerie Gailus-Durner, Ella Dragileva, Larissa Haliw, Ildiko Racz, Wolfgang Wurst, Klaus Ruether, Martin Klingenspor, Martin Hrabě de Angelis, Jochen Graw, Thure Adler
Publikováno v:
PLoS ONE
PLoS ONE 7:e38310 (2012)
PLOS ONE 7(6), e38310 (2012). doi:10.1371/journal.pone.0038310
PLoS ONE, Vol 7, Iss 6, p e38310 (2012)
PLoS ONE 7:e38310 (2012)
PLOS ONE 7(6), e38310 (2012). doi:10.1371/journal.pone.0038310
PLoS ONE, Vol 7, Iss 6, p e38310 (2012)
Cln3(Delta ex7/8) mice harbor the most common genetic defect causing juvenile neuronal ceroid lipofuscinosis (JNCL), an autosomal recessive disease involving seizures, visual, motor and cognitive decline, and premature death. Here, to more thoroughly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2624a6d48c25d6636e5e7eaf2ae31a31
https://doi.org/10.1371/journal.pone.0038310
https://doi.org/10.1371/journal.pone.0038310