PMC:1189074 / 2890-3315
Annnotations
craft-sa-dev
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activity is essential for complete fatty acid oxidation. Inherited MCAD deficiency exists in humans as an autosomal recessive disorder. MCAD deficiency was first described in 1982—1983 [5–7] and has been described in numerous patients [1,8–11]. The carrier frequency in the Caucasian population has been estimated to be between 1 in 50 to 80 with an incidence of clinical disease expected at around 1 in 15,000 [1,9,12]."}
craft-ca-core-dev
{"project":"craft-ca-core-dev","denotations":[{"id":"T821","span":{"begin":40,"end":50},"obj":"CHEBI:35366"},{"id":"T822","span":{"begin":40,"end":60},"obj":"GO:0019395"},{"id":"T823","span":{"begin":51,"end":60},"obj":"MOP:0000568"},{"id":"T824","span":{"begin":98,"end":104},"obj":"NCBITaxon:9606"},{"id":"T825","span":{"begin":111,"end":120},"obj":"GO:0030849"}],"text":"MCAD activity is essential for complete fatty acid oxidation. Inherited MCAD deficiency exists in humans as an autosomal recessive disorder. MCAD deficiency was first described in 1982—1983 [5–7] and has been described in numerous patients [1,8–11]. The carrier frequency in the Caucasian population has been estimated to be between 1 in 50 to 80 with an incidence of clinical disease expected at around 1 in 15,000 [1,9,12]."}
2_test
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craft-ca-core-ex-dev
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