FGFR3 mutation causes abnormal membranous ossification in achondroplasia
FGFR3 gain-of-function mutations lead to both chondrodysplasias and craniosynostoses. Achondroplasia (ACH), the most frequent dwarfism, is due to an FGFR3-activating mutation which results in impaired endochondral ossification. The effects of the mutation on membranous ossification are unknown. Fgfr...
Tallennettuna:
| Päätekijät: | , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | englanti |
| Julkaistu: |
2014
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| Linkit: | https://doi.org/10.1093/hmg/ddu004 |
| Tagit: |
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