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1: Hum Mol Genet. 1995 Nov;4(11):2175-7.Click here to read Links

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

Department of Biological Chemistry, University of California, Irvine 92717, USA.

PMID: 8589699 [PubMed - indexed for MEDLINE]