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ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome
ArticleAbstract: Peters plus syndrome (MIM #261540 PTRPLS), characterized by defects in eye development, prominent foPalabras claves:Autores:Apte S.S., Berardinelli S.J., Cameron D.C., David Edward Komatsu, Dubail J., Grady R.C., Haltiwanger R.S., Holdener B.C., Honkanen R., Jimenez-Vega J.C., McClain S.A., Narimatsu H., Neupane S., Percival C.J., Sato T., Takeuchi M., Uddin S.M.Z., Zhang A.Fuentes:scopusErratum: ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome (Human Molecular Genetics (2019) 28:24 (4053-4066) DOI: 10.1093/hmg/ddz225)
OtherAbstract: The authors wish to apologize for errors in B3glct Tm1Nari allele nomenclature in the above article.Palabras claves:Autores:Apte S.S., Berardinelli S.J., Cameron D.C., David Edward Komatsu, Dubail J., Grady R.C., Haltiwanger R.S., Holdener B.C., Honkanen R., Jimenez-Vega J.C., McClain S.A., Narimatsu H., Neupane S., Percival C.J., Sato T., Takeuchi M., Uddin S.M.Z., Zhang A.Fuentes:scopus