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The disease process changes the environment of the whole pelvic bowl, leading to chronic inflammation and adhesions in the surrounding structures

Buyske S, Williams TA, Mars AE, Stenroos ES, Ming SX, Wang R, Sreenath M, Factura MF, Reddy C, Lambert GH, Johnson WG: Analysis of case-parent trios at a locus with a deletion allele association of GSTM1 with autism

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The 5-UTR mutation of the human HR gene causes a rare autosomal dominant alopecia disease: Marie Unna hereditary hypotrichosis (MUHH), which is characterized by an abnormal hair density on the scalp, eyebrows, eyelashes, or body