KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect

Metz, Kyle A.; Teng, Xinchen; Coppens, Isabelle; Lamb, Heather M.; Wagner, Bart E.; Rosenfeld, Jill A.; Chen, Xianghui; Zhang, Yu; Kim, Hee Jong; Meadow, Michael E.; Wang, Tim Sen; Haberlandt, Edda D.; Anderson, Glenn W.; Leshinsky-Silver, Esther; Bi, Weimin; Markello, Thomas C.; Pratt, Marsha; Makhseed, Nawal; Garnica, Adolfo; Danylchuk, Noelle R.; Burrow, Thomas A.; Jayakar, Parul; McKnight, Dianalee; Agadi, Satish; Gbedawo, Hatha; Stanley, Christine; Alber, Michael; Prehl, Isabelle; Peariso, Katrina; Ong, Min Tsui; Mordekar, Santosh R.; Parker, Michael J.; Crooks, Daniel; Agrawal, Pankaj B.; Berry, Gerard T.; Loddenkemper, Tobias; Yang, Yaping; Maegawa, Gustavo H. B.; Aouacheria, Abdel; Markle, Janet G.; Wohlschlegel, James A.; Hartman, Adam L.; Hardwick, J. Marie

KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect

Autor(en):

Metz, Kyle A.; Teng, Xinchen; Coppens, Isabelle; Lamb, Heather M.; Wagner, Bart E.; Rosenfeld, Jill A.; Chen, Xianghui; Zhang, Yu; Kim, Hee Jong; Meadow, Michael E.; Wang, Tim Sen; Haberlandt, Edda D.; Anderson, Glenn W.; Leshinsky-Silver, Esther; Bi, Weimin; Markello, Thomas C.; Pratt, Marsha; Makhseed, Nawal; Garnica, Adolfo; Danylchuk, Noelle R.; Burrow, Thomas A.; Jayakar, Parul; McKnight, Dianalee; Agadi, Satish; Gbedawo, Hatha; Stanley, Christine; Alber, Michael; Prehl, Isabelle; Peariso, Katrina; Ong, Min Tsui; Mordekar, Santosh R.; Parker, Michael J.; Crooks, Daniel; Agrawal, Pankaj B.; Berry, Gerard T.; Loddenkemper, Tobias; Yang, Yaping; Maegawa, Gustavo H. B.; Aouacheria, Abdel; Markle, Janet G.; Wohlschlegel, James A.; Hartman, Adam L.; Hardwick, J. Marie

Tübinger Autor(en):

Alber, Michael Wolfgang Hans-Peter

Erschienen in:

Annals of Neurology (2018), Bd. 84, H. 5, S. 766-780

Verlagsangabe:

Wiley

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1002/ana.25351

ISSN:

1531-8249