Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Simona K. Zahova"'
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Prader-Willi Syndrome (PWS) is a neurodevelopmental disorder caused by mutations affecting paternal chromosome 15q11-q13, and characterized by hypotonia, hyperphagia, impaired cognition, and behavioural problems. Psychotic illness is a chall
Externí odkaz:
https://doaj.org/article/bfe9406a565643728a0bb57272fc6102
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-11 (2021)
Translational Psychiatry
Translational Psychiatry
Prader-Willi Syndrome (PWS) is a neurodevelopmental disorder caused by mutations affecting paternal chromosome 15q11-q13, and characterized by hypotonia, hyperphagia, impaired cognition, and behavioural problems. Psychotic illness is a challenging pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefc9ed78d025f2ab22bd8de4560dc84
https://orca.cardiff.ac.uk/id/eprint/143275/2/s41398-021-01561-x.pdf
https://orca.cardiff.ac.uk/id/eprint/143275/2/s41398-021-01561-x.pdf
Autor:
Simona K. Zahova, Anthony Roger Isles
Publikováno v:
Epigenomes, Vol 2, Iss 4, p 18 (2018)
Prader-Willi Syndrome (PWS) is a neurodevelopmental disorder caused by loss of expression of the paternally inherited genes on chromosome 15q11.2-q13. However, the core features of PWS have been attributed to a critical interval (PWS-cr) within the 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::403db3bddae09942a40270e793bf4bfb
https://doi.org/10.3390/epigenomes2040018
https://doi.org/10.3390/epigenomes2040018