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Published in 2023 at "Genes"
DOI: 10.3390/genes14010199
Abstract: Achondroplasia is an autosomal dominant genetic disease representing the most common form of human skeletal dysplasia: almost all individuals with achondroplasia have identifiable mutations in the fibroblast growth factor receptor type 3 (FGFR3) gene. The…
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Keywords:
abilities nutritional;
expect feeding;
aspects achondroplasia;
achondroplasia patients ... See more keywords