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Common Symptoms Of Gitelman SyndromeThe cause of Gitelman syndrome is a mutation or alteration in the code on an individual's SLC12A3 gene inherited from a family member in an autosomal recessive fashion. Unlike other salt-wasting ...
Inherited disorders caused by a single abnormal gene are transmitted to offspring in a predictable fashion, termed Mendelian transmission ... inherited by simple patterns classified as autosomal ...
Recessive traits may skip generations and will affect both genders equally. An example of an autosomal recessive condition is cystic fibrosis. Cystic fibrosis close cystic fibrosisA disorder that ...
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