ITCH deficiency clinical phenotype expansion and mitochondrial dysfunction.

Authors:
Wolfe R; Heiman P; D'Annibale O; Karunanidhi A; Powers A and 8 more

Journal:
Mol Genet Metab Rep

Publication Year: 2022

DOI:
10.1016/j.ymgmr.2022.100932

PMCID:
PMC9634006

PMID:
36338154

View on PubMed View on PMC View Publisher
Journal Information

Full Title: Mol Genet Metab Rep

Abbreviation: Mol Genet Metab Rep

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Genetics & Heredity

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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"Author disclosures The authors have no competing interests to declare."

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"Funding LGG is funded in part by the 10.13039/100000051National Human Genome Research Institute (NHGRI) grant #K08 HG010490, a component of the 10.13039/100000002National Institutes of Health (NIH). The contents of this manuscript are solely the responsibility of the authors and do not necessarily represent the official view of NHGRI/NIH."

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Last Updated: Aug 05, 2025