Galactosemia is an inherited disorder in humans. A person with the disorder cannot digest the sugars in milk. The allele for normal digestion (G) is dominant; the allele for galactosemia (g) is recessive. A female who is heterozygous for the galactosemia trait and a male who has galactosemia have a child. In your response, be sure to: Identify the genotypes of the mother and father
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The protein(s) that are the major contributors to plasma osmolarity is/are
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Galactosemia is an inherited disorder in humans. A person with the disorder cannot digest the sugars...
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