NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis

Thyroid hemiagenesis (THA) is an inborn absence of one thyroid lobe of largely unknown etiopathogenesis. The aim of the study was to reveal genetic factors responsible for thyroid maldevelopment in two siblings with THA. None of the family members presented with congenital heart defect. The samples...

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Detalles Bibliográficos
Autores principales: Szczepanek-Parulska, Ewelina, Budny, Bartłomiej, Borowczyk, Martyna, Zhukov, Igor, Szutkowski, Kosma, Zawadzka, Katarzyna, Tahir, Raiha, Minczykowski, Andrzej, Niedziela, Marek, Ruchała, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8950672/
https://www.ncbi.nlm.nih.gov/pubmed/35328834
http://dx.doi.org/10.3390/ijms23063414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8950672/
https://www.ncbi.nlm.nih.gov/pubmed/35328834
http://dx.doi.org/10.3390/ijms23063414

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