DTDSTDiastrophic Dysplasia Sulfate Transporter
References in periodicals archive ?
The diagnosis of DTDST deficiency can be confirmed at the molecular genetic level (122-125).
Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279W.
Recessively inherited multiple epiphyseal dysplasia with normal stature, club foot, and double layered patella caused by a DTDST mutation.