Genetic variation in the HTR1A gene and sudden infant death syndrome

Megan E. Morley; Casey M. Rand; Elizabeth M. Berry-Kravis; Lili Zhou; Wenqing Fan; Debra E. Weese-Mayer

doi:10.1002/ajmg.a.32112

Genetic variation in the HTR1A gene and sudden infant death syndrome

Megan E. Morley, Casey M. Rand, Elizabeth M. Berry-Kravis, Lili Zhou, Wenqing Fan, Debra E. Weese-Mayer

Pediatrics

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Original language	English (US)
Pages (from-to)	930-933
Number of pages	4
Journal	American Journal of Medical Genetics, Part A
Volume	146
Issue number	7
DOIs	https://doi.org/10.1002/ajmg.a.32112
State	Published - Apr 1 2008

ASJC Scopus subject areas

Genetics(clinical)
Genetics

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1002/ajmg.a.32112

Cite this

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title = "Genetic variation in the HTR1A gene and sudden infant death syndrome",

author = "Morley, {Megan E.} and Rand, {Casey M.} and Berry-Kravis, {Elizabeth M.} and Lili Zhou and Wenqing Fan and Weese-Mayer, {Debra E.}",

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T1 - Genetic variation in the HTR1A gene and sudden infant death syndrome

AU - Morley, Megan E.

AU - Rand, Casey M.

AU - Berry-Kravis, Elizabeth M.

AU - Zhou, Lili

AU - Fan, Wenqing

AU - Weese-Mayer, Debra E.

PY - 2008/4/1

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SN - 1552-4825

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JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

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Genetic variation in the HTR1A gene and sudden infant death syndrome

ASJC Scopus subject areas

UN SDGs

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