Associated Papers
Structural effect of the H992D/H418D mutation of angiotensin-converting enzyme in the Indian population: implications for health and disease.
Kulshreshtha A et al.
Journal of Biomolecular Structure & Dynamics, 2025
XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
Piton A et al.
American Journal of Human Genetics, 2013
Sequence variations in AGTR2 are unlikely to be associated with X-linked mental retardation.
Huang D et al.
American Journal of Medical Genetics. Part A, 2005
Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation.
Ylisaukko-oja T et al.
Human Genetics, 2004
Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardation.
Bienvenu T et al.
Journal of Medical Genetics, 2003
AGTR2 mutations in X-linked mental retardation.
Vervoort VS et al.
Science (new York, N.y.), 2002
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