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Hum Mol Genet. 1995 Nov;4(11):2175-7.

Another mutation that results in the substitution of an unpaired cysteine residue in the extracellular domain of FGFR3 in thanatophoric dysplasia type I.

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  • 1Department of Biological Chemistry, University of California, Irvine 92717, USA.
PMID:
8589699
[PubMed - indexed for MEDLINE]
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