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A recurrent mutation in the tyrosine kinase domain of fib... | ResearchHub
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A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
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Authors
Gary Bellus
8 more
Gary Bellus
•
Iain McIntosh
6 more
•
Clair Francomano
Published
July 1, 1995
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Journal
Nature Genetics
Topics
Biology
Genetics
Molecular Biology
Mutation
Mutant
Show all topics
DOI
10.1038/ng0795-357
