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pro vyhledávání: '"Vuong Tran, Nguyen Quoc"'
Autor:
Nakamura, Yuki, Urakami, Takeo, Ishimaru, Kayoko, Vuong Tran, Nguyen Quoc, Shimizu, Takafumi, Sinko, William, Takahashi, Taisuke, Marappan, Sivapriya, Narayanan, Kishore, Poddutoori, Ramulu, Terada, Yoh, Nakao, Atsuhito
Publikováno v:
In Journal of Allergy and Clinical Immunology: Global August 2024 3(3)
Publikováno v:
Diseases, Vol 4, Iss 1, p 15 (2016)
Prader-Willi syndrome (PWS) is a congenital neurodevelopmental disorder caused by loss of function of paternally expressed genes on chromosome 15 due to paternal deletion of 15q11–q13, maternal uniparental disomy for chromosome 15, or an imprinting
Externí odkaz:
https://doaj.org/article/b9f54e17d26f4b68b500674de297e9de
Publikováno v:
Diseases, Vol 4, Iss 1, p 15 (2016)
Diseases
Diseases
Prader-Willi syndrome (PWS) is a congenital neurodevelopmental disorder caused by loss of function of paternally expressed genes on chromosome 15 due to paternal deletion of 15q11-q13, maternal uniparental disomy for chromosome 15, or an imprinting m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff52102d84da13745569b36276c1e740
https://doi.org/10.3390/diseases4010015
https://doi.org/10.3390/diseases4010015