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Updated: Jul 7, 2026

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Genetic variation in the HTR1A gene and sudden infant death syndrome
Megan E Morley1, Casey M Rand, Elizabeth M Berry-Kravis
1Department of Pediatrics, Rush Children's Hospital at Rush University Medical Center, Chicago, Illinois 60612, USA.
American Journal of Medical Genetics. Part A
|February 21, 2008
Abstract
No abstract available in PubMed .
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