Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Vera Splittstoesser"'
Autor:
Vera Splittstoesser, Heike Vollbach, Michaela Plamper, Werner Garbe, Elisa De Franco, Jayne A. L. Houghton, Gesche Dueker, Rainer Ganschow, Bettina Gohlke, Felix Schreiner
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundNeonatal diabetes with congenital hypothyroidism (NDH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the GLI-similar 3 coding gene GLIS3. Almost 20 patients have been reported to date, with signific
Externí odkaz:
https://doaj.org/article/2c4c6cfa982f459988f2117f3d8b8ff1
Autor:
Elisa De Franco, Michaela Plamper, Felix Schreiner, Vera Splittstoesser, Werner Garbe, Heike Vollbach, Gesche Dueker, Jayne A L Houghton, Bettina Gohlke, Rainer Ganschow
Publikováno v:
Frontiers in Endocrinology
Frontiers in Endocrinology, Vol 12 (2021)
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundNeonatal diabetes with congenital hypothyroidism (NDH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the GLI-similar 3 coding gene GLIS3. Almost 20 patients have been reported to date, with signific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbaa2a9dc7cf6646ac71d4c5eabc746c
http://europepmc.org/articles/PMC8087289
http://europepmc.org/articles/PMC8087289