Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion

PURPOSE: Prader-Willi syndrome (PWS) is a well-known genetic disorder, and microdeletion on chromosome 15 is the most common causal mechanism. Several previous studies have suggested that various environmental factors might be related to the pathogenesis of microdeletion in PWS. In this study, we in...

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Detalles Bibliográficos
Autores principales: Yang, Aram, Lee, Yeon Hee, Nam, Soon Young, Jeong, Yu Ju, Kyung, Yechan, Huh, Rimm, Lee, Jieun, Kwun, Younghee, Cho, Sung Yoon, Jin, Dong-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397272/
https://www.ncbi.nlm.nih.gov/pubmed/25883926
http://dx.doi.org/10.6065/apem.2015.20.1.40

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