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Correlation of ATP7B gene mutations with clinical phenotype and radiological features in Indian Wilson disease patients.

Acta neurologica Belgica - 1 Feb 2022

Chaudhuri Jasodhara, Biswas Samar, Gangopadhyay Goutam, Biswas Tamoghna, Datta Jyotishka, Biswas Atanu, Pandit Alak, Datta Amlan Kusum, Mukherjee Adreesh, Dutta Atanu Kumar, Bhattacharya Paramita, Hazra Avijit

Abstract excerpt

INTRODUCTION: Wilson disease (WD) is characterized by a wide variety of clinical manifestations. Our study aimed to correlate genotype with clinical and radiological features in Indian WD patients. METHODS: We conducted a descriptive observational study in a tertiary care neurology referral center of eastern India over a period of 2 years. Demographic data collection, clinical examination and relevant...

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PMID: 34643937
DOI: 10.1007/s13760-021-01816-w

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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