Zobrazeno 1 - 2
of 2
pro vyhledávání: '"L-R asymmetry defects"'
Autor:
Andrea Bieder, Elisabet Einarsdottir, Hans Matsson, Harriet E. Nilsson, Jesper Eisfeldt, Anca Dragomir, Martin Paucar, Tobias Granberg, Tie-Qiang Li, Anna Lindstrand, Juha Kere, Isabel Tapia-Páez
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Developmental dyslexia (DD) is a neurodevelopmental learning disorder with high heritability. A number of candidate susceptibility genes have been identified, some of which are linked to the function of the cilium, an organelle re
Externí odkaz:
https://doaj.org/article/5544082e59974e9a9eb410d7ba08276a
Autor:
Martin Paucar, Anca Dragomir, Tie-Qiang Li, Harriet Nilsson, Elisabet Einarsdottir, Juha Kere, Anna Lindstrand, Tobias Granberg, Hans Matsson, Andrea Bieder, Jesper Eisfeldt, Isabel Tapia-Páez
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
BackgroundDevelopmental dyslexia (DD) is a neurodevelopmental learning disorder with high heritability. A number of candidate susceptibility genes have been identified, some of which are linked to the function of the cilium, an organelle regulating l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cb27fa8c2ee5534f56ea5996d8e28c4
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413235
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413235
