Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield syndrome

Heterozygous kinase domain mutations or homozygous extracellular domain mutations in FGFR1 have been reported to cause Hartsfield syndrome (HS), which is characterized by the triad of holoprosencephaly, ectrodactyly and cleft lip/palate. To date, more than 200 mutations in FGFR1 have been described;...

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Detalles Bibliográficos
Autores principales: Takagi, Masaki, Miyoshi, Tatsuya, Nagashima, Yuka, Shibata, Nao, Yagi, Hiroko, Fukuzawa, Ryuji, Hasegawa, Tomonobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061861/
https://www.ncbi.nlm.nih.gov/pubmed/27790375
http://dx.doi.org/10.1038/hgv.2016.34

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061861/
https://www.ncbi.nlm.nih.gov/pubmed/27790375
http://dx.doi.org/10.1038/hgv.2016.34

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