Work

A microdeletion in Xp11.3 accounts for co‐segregation of retinitis pigmentosa and mental retardation in a large kindred

Year: 2006

Type: article

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.31080

Authors: Lilei Zhang, Tao Wang, Alan F. Wright, Mohnish Suri, Charles E. Schwartz, Roger E. Stevenson, David Valle

Institutions: Johns Hopkins University, Johns Hopkins Medicine, Western General Hospital, MRC Human Genetics Unit, Nottingham City Hospital, Greenwood Genetic Center, Howard Hughes Medical Institute

Language: English

Topic: Retinal Development and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G2752626688, Mental Retardation and Developmental Disabilities Research Centers 2008, ID of Genes Responsible for X-Linked Mental Retardation

OpenAlex ID: W2054496491

FWCI: 0.543

Cites: 33

Cited by: 24

Related to: 10