3 results for author:"Miertus J." in Literature citations
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| Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. Michalk A., Stricker S., Becker J., Rupps R., Pantzar T., Miertus J., Botta G., Naretto V.G., Janetzki C., Yaqoob N. et al. Am. J. Hum. Genet. 82:464-476(2008) · UniProtKB (3) · Mapped (25) |
| Molecular aspects of a novel HLA-A*02 allele (A*0297): the first HLA class I allele mutated at codon 232. Garino E., Miertus J., Berrino M., Bertinetto F., Caropreso P., Gay V., Mazzola G., Tondat F., Frecer V., Miertus S. et al. Tissue Antigens 69:342-347(2007) · Mapped (449) |
| A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndrome. Miertus J., Borozdin W., Frecer V., Tonini G., Bertok S., Amoroso A., Miertus S., Kohlhase J. Hum. Genet. 119:154-161(2006) · UniProtKB (1) |