Mutation Screening of the HGD Gene Identifies a Novel Alkaptonuria Mutation with Significant Founder Effect and High Prevalence - Sakthivel - 2014 - Annals of Human Genetics - Wiley Online Library
PDF) A Novel Missense HGD Gene Mutation, K57N, in a Patient with Alkaptonuria | Jeffrey Wade Brown, MD, PhD - Academia.edu
Homogentisate 1,2-dioxygenase - an overview | ScienceDirect Topics
Location of the nine possible SNPs along the bovine HGD gene. Black... | Download Scientific Diagram
A novel mutation in the homogentisate 1,2 dioxygenase gene identified in Chinese Hani pediatric patients with Alkaptonuria - ScienceDirect
Homogentisate 1,2-dioxygenase - an overview | ScienceDirect Topics
HGD siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
HGDiscovery: an online tool providing functional and phenotypic information on novel variants of homogentisate 1,2- dioxigenase | bioRxiv
Homogentisate 1,2-dioxygenase (HGD) gene variants, their analysis and genotype–phenotype correlations in the largest cohort of patients with AKU | European Journal of Human Genetics
Alkaptonuria - General Information
Avraham Z. Cooper, MD on X: "RT @DrJamielinho: @AvrahamCooperMD Alkaptonuria: inherited genetic disorder characterized by a mutation in the HGD gene and subsequent homo…" / X
Alkaptonuria - Wikipedia
Novel R225C variant identified in the HGD gene in Jordanian patients with alkaptonuria