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pro vyhledávání: '"Christine Raybaud"'
Autor:
Juliane Leger, Didier Lacombe, Aurore Carré, Hubert Ythier, Elodie Tron, Sylvia Sura-Trueba, Michel Polak, Serge Romana, Marie-Laure Moutard, Catherine Raynaud-Ravni, Isabelle Broutin-L'Hermite, Mireille Castanet, Gabor Szinnai, Christine Raybaud, Cyril Goizet, Pascal Barat
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2009, 18 (12), pp.2266-2276. ⟨10.1093/hmg/ddp162⟩
Human Molecular Genetics, Oxford University Press (OUP), 2009, 18 (12), pp.2266-2276. ⟨10.1093/hmg/ddp162⟩
Thyroid transcription factor 1 (NKX2-1/TITF1) mutations cause brain-lung-thyroid syndrome, characterized by congenital hypothyroidism (CH), infant respiratory distress syndrome (IRDS) and benign hereditary chorea (BHC). The objectives of the present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4f57fcc311401975b2bd4f4d283171c
https://hal.archives-ouvertes.fr/hal-02519920
https://hal.archives-ouvertes.fr/hal-02519920