Mutation Screening of theHGDGene Identifies a Novel Alkaptonuria Mutation with Significant Founder Effect and High Prevalence-Reference-Cited by-同舟云学术

Mutation Screening of theHGDGene Identifies a Novel Alkaptonuria Mutation with Significant Founder Effect and High Prevalence

Author:

Sakthivel Srinivasan¹,Zatkova Andrea²,Nemethova Martina²,Surovy Milan³,Kadasi Ludevit²³,Saravanan Madurai P.⁴

Affiliation:

1. Department of Biotechnology & Genetic Engineering; Bharathidasan University; Tiruchirapalli Tamil Nadu India

2. Institute of Molecular Physiology and Genetics; Slovak Academy of Sciences; Vlarska 5 Bratislava Slovakia

3. Department of Molecular Biology; Faculty of Natural Sciences; Comenius University; Mlynskadolina Bratislava Slovakia

4. Department of Biochemistry; KAP Viswanatham Government Medical College; Tiruchirapalli Tamil Nadu India

Funder

Creating a Competitive Centre for Research and Development in the Field of Molecular Medicine

Research & Developmental Operational Programme

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference44 articles.

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1. Alkaptonuria;Nature Reviews Disease Primers;2024-03-07

2. Alkaptonuria;Genetic Syndromes;2023