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pro vyhledávání: '"Andy Saurin"'
Autor:
Laurent Fasano, Colette Denis, Guylène Feuillet, Andy Saurin, Ahmed Fatmi, Thien Phong Vu Manh, Petra Zürbig, Joost P. Schanstra, Irene Sanchez-Martin, Xavier Caubit, Fabrice Richard, Pedro Magalhães
Renal tract defects and autism spectrum disorder (ASD) deficits represent the phenotypic core of the 19q12 deletion syndrome caused by the loss of one copy of the TSHZ3 gene. While a proportion of Tshz3 heterozygous (Tshz3+/lacZ) mice display uretera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7fa07821ba7d49d9e9d4985e463b7f5
https://halshs.archives-ouvertes.fr/halshs-03410717
https://halshs.archives-ouvertes.fr/halshs-03410717
