NGLY1 mutations cause protein aggregation in human neurons-Reference-Cited by-同舟云学术

NGLY1 mutations cause protein aggregation in human neurons

Published:2023-12 Issue:12 Volume:42 Page:113466
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Manole Andreea,Wong Thomas,Rhee Amanda,Novak Sammy^ORCID,Chin Shao-Ming,Tsimring Katya^ORCID,Paucar Andres,Williams April^ORCID,Newmeyer Traci Fang,Schafer Simon T.,Rosh Idan,Kaushik Susmita,Hoffman Rene,Chen Songjie,Wang Guangwen,Snyder Michael,Cuervo Ana Maria,Andrade Leo,Manor Uri^ORCID,Lee Kevin^ORCID,Jones Jeffrey R.,Stern Shani^ORCID,Marchetto Maria C.,Gage Fred H.^ORCID

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference57 articles.

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4. Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation;Lam;Genet. Med.,2017

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