Work

Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome

Year: 2006

Type: article

Source: The American Journal of Human Genetics

DOI: 10.1086/508474

Authors: Isabella Wimplinger, Manuela Morleo, Georg Rosenberger, Daniela Iaconis, Ulrike Orth, Peter Meinecke, Israela Lerer, Andrea Ballabio, Andreas Gal, Brunella Franco, Kerstin Kutsche

Institutions: University Medical Center Hamburg-Eppendorf, Telethon Institute Of Genetics And Medicine, University of Naples Federico II, Altonaer Kinderkrankenhaus, Hadassah Medical Center, Federico II University Hospital

Language: English

Topic: Mitochondrial Function and Pathology

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funder: University of Rochester

OpenAlex ID: W1972593650

FWCI: 2.455

Cites: 57

Cited by: 164

Related to: 10