Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Bengt Engerström"'
Publikováno v:
Brain and Development. 35:270-273
Rett syndrome (RS) is a unique X-linked dominant neurodevelopmental disorder affecting 1 in 10,000 females. Mutations in the MECP2 gene located on Xq28 have been identified. Many of the characteristic features evolve due to immaturity of the brain in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a8f098d9b8e239f4ab1a3acfb7d7905
https://doi.org/10.1016/j.braindev.2012.04.004
https://doi.org/10.1016/j.braindev.2012.04.004
Autor:
Peter O.O. Julu, Giorgio Pini, Eric Smeets, Robert S. Delamont, Flora Apartopoulos, Ingegerd Witt Engerström, Stig Hansen, Bengt Engerström
Publikováno v:
The Lancet. 371:1981-1983
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fde1cf685df33093ba118aa26b57452
https://doi.org/10.1016/s0140-6736(08)60849-1
https://doi.org/10.1016/s0140-6736(08)60849-1