Natural history of NGLY1 deficiency: motor function & clinical features.

Morrison G, Dwight S, Landy H, Mueller WF, Ventola P, Deck R, Schweighardt B, Wilsey M, Lee KJ, Suter B

DOI: 10.1093/hmg/ddag013
Published: 2026 May 11
Container: Human molecular genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1093/hmg/ddag013,
  title = {Natural history of NGLY1 deficiency: motor function \& clinical features.},
  author = {Morrison G and Dwight S and Landy H and Mueller WF and Ventola P and Deck R and Schweighardt B and Wilsey M and Lee KJ and Suter B},
  year = {2026},
  journal = {Human molecular genetics},
  doi = {10.1093/hmg/ddag013},
  url = {https://doi.org/10.1093/hmg/ddag013}
}

RIS

TY  - JOUR
TI  - Natural history of NGLY1 deficiency: motor function & clinical features.
AU  - Morrison G
AU  - Dwight S
AU  - Landy H
AU  - Mueller WF
AU  - Ventola P
AU  - Deck R
AU  - Schweighardt B
AU  - Wilsey M
AU  - Lee KJ
AU  - Suter B
PY  - 2026
JO  - Human molecular genetics
DO  - 10.1093/hmg/ddag013
UR  - https://doi.org/10.1093/hmg/ddag013
ER  -

APA

G, M., S, D., H, L., WF, M., P, V., R, D., B, S., M, W., KJ, L., & B, S. (2026). Natural history of NGLY1 deficiency: motor function & clinical features.. Human molecular genetics. https://doi.org/10.1093/hmg/ddag013

Source records

pubmed · retrieved 2026-09-26T08:32:05.543Z