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pro vyhledávání: '"Birgit Halm"'
Autor:
Birgit Halm, Karl Deisseroth, Joseph H. Bayle, Feng Ding, Katharine C. Harrison, Madhuri Roy, Hong Hua Li, Unsal Kuscuoglu, Corinne M. Spencer, Uta Francke, Leslie Meltzer, Richard Paylor, Elena E. Wright, Alessandra Splendore
Publikováno v:
EMBO Molecular Medicine
The neurodevelopmental disorder Williams-Beuren syndrome is caused by spontaneous approximately 1.5 Mb deletions comprising 25 genes on human chromosome 7q11.23. To functionally dissect the deletion and identify dosage-sensitive genes, we created two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ce0fd14cc36eb6ed436dac3b6fcb408
https://doi.org/10.1002/emmm.200900003
https://doi.org/10.1002/emmm.200900003
