https://www.selleckchem.com/pr....oducts/4-aminobutyri
0051; OR 0,312 [0,143-0,721]) in MRS patients compared with the control group. Crohn disease (CD) patients had disparate genetic profiles versus those with MRS. This single-institution study had a small cohort, because this disease is rare. Conclusions There is a genetic predisposition toward MRS, involving associated and protective genes. Interstitial deletions of 16q chromosome including 16q12.1q21 region are very rare, with only three cases reported to date. Main clinical features include dysmorphisms, short stature, micr
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