An unusual case of hereditary transthyretin‐related amyloidosis and ulcerative colitis in a young Indian girl
Author:
Affiliation:
1. Department of GastroenterologyPostgraduate Institute of Medical Education and Research Chandigarh India
2. Department of PaediatricsPostgraduate Institute of Medical Education and Research Chandigarh India
Publisher
Wiley
Subject
Gastroenterology,Hepatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgh3.12206
Reference9 articles.
1. Familial amyloid polyneuropathy in Taiwan: Identification of transthyretin variant (Leu55 → Pro)
2. THAOS: Gastrointestinal manifestations of transthyretin amyloidosis - common complications of a rare disease
3. Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype–phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden
4. FAP in India: a first genetically proven case
5. Transthyretin mutation Leu-55-Pro significantly alters tetramer stability and increases amyloidogenicity
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