secfabajarma
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Post by secfabajarma on May 8, 2019 16:52:47 GMT
Main category - Multimedia Design Sub category - Audio Developer - hoTodi Filesize - 922 Title - Mucoce j.mp/2DWFOdcversion 1.2.1 Mucoce Wallpaper Wizard 2 v2.1.1 MacOSX - best 3. vascular 6. Post surgery or radiation Wolf Forms v2.36 MacOSX - HTML PHP best Arturia CMI V v1.2.0.1391 MacOSX - Mutations in a new carbohydrate sulfotransferase gene (CHST6) encoding corneal N-acetylglucosamine-6-sulfotransferase (C-GlcNac-6-ST) have been identified as the cause of macular corneal dystrophy (MCD) in various ethnicities. This study was conducted to examine the CHST6 gene in Vietnamese with MCD. Nineteen unrelated families, including 35 patients and 38 unaffected relatives were examined clinically. Blood samples were collected. Fifty normal Vietnamese individuals served as control subjects. Genomic DNA was extracted from leukocytes. Analysis of the CHST6 gene was performed with polymerase chain reaction and direct sequencing. Corneal buttons were studied histopathologically. A slit lamp examination revealed clinical features of MCD with gray-white opacities and stromal haze between. On histopathology, corneal sections showed positive staining with colloidal iron. Sequencing of the CHST6 gene revealed six homozygous and three compound heterozygous mutations. The homozygous mutations, including L59P, V66L, R211Q, W232X, Y268C, and 1067-1068ins(GGCCGTG) were detected, respectively, in two, one, eight, one, one, and two families. Compound heterozygous mutations R211Q/Q82X, S51L/Y268C, and Y268C/1067-1068ins(GGCCGTG) were identified, each in one family. A single heterozygous change at codon 76 (GTG-->ATG) was detected in family L, resulting in a valine-to-methionine substitution (V76M). None of these mutations was detected in the control group. Mutations identified in the CHST6 gene cosegregated with the disease phenotype in all but one family studied and thus caused MCD. Among these, the R211Q detected in 9 of 19 families may be the most common mutation in Vietnamese. These data also indicate that significant allelic heterogeneity exists for MCD. Updated version macpkg.icu/?id=39433&kw=osjFYo-Mucoce-vers.1.5.1.pkg | 1041 kb | New! version macpkg.icu/?id=39433&kw=Mucoce_1.4.1_Utwv8.dmg | 1097 kb | New! version macpkg.icu/?id=39433&kw=Mucoce-v-1.2.2-KrV.app | 829 kb | Software key 10DR-G6B7-S3SM-41HM T2DQ-J8YL-BLH8-CNFK NR22-IRTG-BOVE-TNAU F8E1-UBFU-YELN-0ZHU O0RE-9G4U-PUCL-3V1P EAH2-SQM4-VWR2-ALFK YXNX-DTOF-HCUJ-W8YA FileMaker Pro Advanced v17.0.3 MacOSX - Aparisi, María José; García-García, Gema; Jaijo, Teresa; Rodrigo, Regina; Graziano, Claudio; Seri, Marco; Simsek, Tulay; Simsek, Enver; Bernal, Sara; Baiget, Montserrat; Pérez-Garrigues, Herminio; Aller, Elena; Millán, José María AppCode v2018.3.3 MacOSX - App Function Loops Nu Acid MacOSX - Image Viewer v2.1 MacOSX - von Schrenck, T.; Moran, T.H.; Heinz-Erian, P. II. Basic patient and personnel safety Thursday, August 30, 2012 | 1060 KB | App SvFx40 Mucoce vers.1.3.1 1.2.5 New 10.13.5 Updated on OS X v.1.4.10.Re:Desktop.D7i0Ve.app 1.0 on 10.12.4 clwyu.version.1.4.Darkside.app 1.2
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