ºÝºÝߣshows by User: bet1986 / http://www.slideshare.net/images/logo.gif ºÝºÝߣshows by User: bet1986 / Sun, 25 Oct 2009 08:54:45 GMT ºÝºÝߣShare feed for ºÝºÝߣshows by User: bet1986 Hemochromatosis Cesmed Betsy Carpio Menautt https://es.slideshare.net/slideshow/hemochromatosis-cesmed-betsy-carpio-menautt/2340880 hemochromatosis-cesmed-betsycarpiomenautt-091025085500-phpapp01
Hereditary hemochromatosis is an autosomal recessive iron-overload disorder associated with mutation of the HFE gene, which is located on chromosome 6; in most cases the mutation is a single-base change that results in the substitution of tyrosine for cysteine at position 282 of the HFE protein (C282Y).]]>
Hereditary hemochromatosis is an autosomal recessive iron-overload disorder associated with mutation of the HFE gene, which is located on chromosome 6; in most cases the mutation is a single-base change that results in the substitution of tyrosine for cysteine at position 282 of the HFE protein (C282Y).]]> Sun, 25 Oct 2009 08:54:45 GMT https://es.slideshare.net/slideshow/hemochromatosis-cesmed-betsy-carpio-menautt/2340880 bet1986@slideshare.net(bet1986) Hemochromatosis Cesmed Betsy Carpio Menautt bet1986 Hereditary hemochromatosis is an autosomal recessive iron-overload disorder associated with mutation of the HFE gene, which is located on chromosome 6; in most cases the mutation is a single-base change that results in the substitution of tyrosine for cysteine at position 282 of the HFE protein (C282Y). <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/hemochromatosis-cesmed-betsycarpiomenautt-091025085500-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Hereditary hemochromatosis is an autosomal recessive iron-overload disorder associated with mutation of the HFE gene, which is located on chromosome 6; in most cases the mutation is a single-base change that results in the substitution of tyrosine for cysteine at position 282 of the HFE protein (C282Y).
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