Work

Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies

Year: 2005

Type: article

Study design: Case Report

Source: Cytogenetic and Genome Research

DOI: 10.1159/000087531

Authors: S.S. Bhat, K.R. Schmidt, S. Ladd, K.C. Kim, C.E. Schwartz, R.J. Simensen, B.R. DuPont, R.E. Stevenson, A.K. Srivastava

Institutions: Greenwood Genetic Center, East Carolina University

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G4785865723, X-Linked Mental Retardation-Linkage

OpenAlex ID: W1980561769

FWCI: 0.18

Cites: 21

Cited by: 26

Related to: 10