Background: Adult-type hypolactasia, the physiological decline of lactase some time after weaning, was previously associated with the LCT -13910C>T polymorphism worldwide except in Africa. Lactase non-persistence is the most common phenotype in humans, except in northwestern Europe with its long history of pastoralism and milking. We had previously shown association of LCT -13910C>T polymorphism with adult-type hypolactasia in Brazilians; thus, we assessed its frequency among different Brazilian ethnic groups. Methods: We investigated the ethnicity-related frequency of this polymorphism in 567 Brazilians [mean age, 42.1 +/- 16.8 years; 157 (27.7%) men]; 399 (70.4%) White, 50 (8.8%) Black, 65 (11.5%) Brown, and 53 (9.3%) Japanese-Brazilian. ...
Recently, the C/T-13910 polymorphism on chromosome 2q21 in North-European populations has been found...
The ability to digest the milk sugar lactose as an adult (lactase persistence) is a variable genetic...
Objectives: To validate C/T-13910 polymorphism associated with primary hypolactasia for clinical pra...
Background: Adult-type hypolactasia, the physiological decline of lactase some time after weaning, w...
Abstract Background ...
Adult-type hypolactasia is a common phenotype caused by the lactase enzyme deficiency. The -13910 C>...
<div><p>Adult-type hypolactasia is a common phenotype caused by the lactase enzyme deficiency. The −...
CONTEXT: Genotyping of single nucleotide polymorphism (SNP C/T-13910) located upstream of the lactas...
Genetically determined deficiency of the lactase enzyme in adults (primary hypolactasia) is a recess...
The Metabolic Syndrome (MetS) is defined as a pattern of metabolic disturbances, which include centr...
The ability to digest the milk sugar lactose as an adult (lactase persistence) is a variable genetic...
The ability to digest the milk sugar lactose as an adult (lactase persistence) is a variable genetic...
The C/T-13910 mutation is the major factor responsible for the persistence of the lactase-phlorizin ...
Adult-type hypolactasia is characterized by the inability to digest lactose during adulthood, due to...
A single-nucleotide variant, C/T-13910, located 14 kb upstream of the lactase gene (LCT), has been s...
Recently, the C/T-13910 polymorphism on chromosome 2q21 in North-European populations has been found...
The ability to digest the milk sugar lactose as an adult (lactase persistence) is a variable genetic...
Objectives: To validate C/T-13910 polymorphism associated with primary hypolactasia for clinical pra...
Background: Adult-type hypolactasia, the physiological decline of lactase some time after weaning, w...
Abstract Background ...
Adult-type hypolactasia is a common phenotype caused by the lactase enzyme deficiency. The -13910 C>...
<div><p>Adult-type hypolactasia is a common phenotype caused by the lactase enzyme deficiency. The −...
CONTEXT: Genotyping of single nucleotide polymorphism (SNP C/T-13910) located upstream of the lactas...
Genetically determined deficiency of the lactase enzyme in adults (primary hypolactasia) is a recess...
The Metabolic Syndrome (MetS) is defined as a pattern of metabolic disturbances, which include centr...
The ability to digest the milk sugar lactose as an adult (lactase persistence) is a variable genetic...
The ability to digest the milk sugar lactose as an adult (lactase persistence) is a variable genetic...
The C/T-13910 mutation is the major factor responsible for the persistence of the lactase-phlorizin ...
Adult-type hypolactasia is characterized by the inability to digest lactose during adulthood, due to...
A single-nucleotide variant, C/T-13910, located 14 kb upstream of the lactase gene (LCT), has been s...
Recently, the C/T-13910 polymorphism on chromosome 2q21 in North-European populations has been found...
The ability to digest the milk sugar lactose as an adult (lactase persistence) is a variable genetic...
Objectives: To validate C/T-13910 polymorphism associated with primary hypolactasia for clinical pra...