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Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects

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Year: 2001
Type: article
Source: Human Molecular Genetics
DOI: 10.1093/hmg/10.22.2549
Author: B. Funke
Institutions: Albert Einstein College of Medicine, Yeshiva University
Language: English

Topic: Congenital Ear and Nasal Anomalies
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute on Deafness and Other Communication Disorders, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: Cochlear Homeostasis, MOLECULAR ASPECTS OF VELO-CARDIO-FACIAL SYNDROME, G398009631, G5760941531, Neurofibromin, Neural Crest and Cardiac Development, G913170246
OpenAlex ID: W2138827141
FWCI: 2.707
Cites: 37
Cited by: 79
Related to: 10
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