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Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder
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Year:
2016
Type:
article
Study design:
Case Report
Source:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2016.05.014
Authors:
Gifty Bhat,
Danielle LaGrave,
Alison Millson,
John Herriges,
Allen N. Lamb,
Reuben Matalon
show all 6
Institutions:
Albert Einstein College of Medicine,
Children's Hospital at Montefiore,
ARUP Laboratories (United States),
University of Utah,
The University of Texas Medical Branch at Galveston
Language:
English
Topic:
Genetics and Neurodevelopmental Disorders
Subfield:
Genetics
Field:
Biochemistry, Genetics and Molecular Biology
Domain:
Life Sciences
SDG:
Good health and well-being
Open Access status:
closed
OpenAlex ID:
W2401548421
FWCI:
2.42
Cites:
19
Cited by:
25
Related to:
10