Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Henrik E, Hagberg"'
Autor:
Regina Vontell, Veena G. Supramaniam, Alice Davidson, Claire Thornton, Andreas Marnerides, Muriel Holder-Espinasse, Suzanne Lillis, Shu Yau, Mattias Jansson, Henrik E. Hagberg, Mary A. Rutherford
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Cytoplasmic Actin Gamma 1 (ACTG1) gene variant are autosomal dominant and can cause CNS anomalies (Baraitser Winter Malformation Syndrome; BWMS). ACTG1 anomalies in offspring include agenesis of the corpus callosum (ACC) and neuronal heterotopia whic
Externí odkaz:
https://doaj.org/article/c70e40fd5db3467286d5de2a9f649edb
Autor:
Regina, Vontell, Veena G, Supramaniam, Alice, Davidson, Claire, Thornton, Andreas, Marnerides, Muriel, Holder-Espinasse, Suzanne, Lillis, Shu, Yau, Mattias, Jansson, Henrik E, Hagberg, Mary A, Rutherford
Publikováno v:
Frontiers in Physiology
Cytoplasmic Actin Gamma 1 (ACTG1) gene variant are autosomal dominant and can cause CNS anomalies (Baraitser Winter Malformation Syndrome; BWMS). ACTG1 anomalies in offspring include agenesis of the corpus callosum (ACC) and neuronal heterotopia whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5cb498183d9610d37304abcaa38af3a6
https://pubmed.ncbi.nlm.nih.gov/31231230
https://pubmed.ncbi.nlm.nih.gov/31231230