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  • WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India.

WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India.

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2022 Apr 19 Others A Chapla, J Johnson, S Korula, N Mohan… - The Journal of …, 2022 - academic.oup.com

Full Author : ['Chapla, Aaron', 'Johnson, Jabasteen', 'Korula, Sophy', 'Mohan, Nisha', 'Ahmed, Anish', 'Varghese, Deny', 'Rangasamy, Parthiban', 'Ravichandran, Lavanya', 'Jebasingh, Felix', 'Kumar Agrawal, Krishna', 'Somasundaram, Noel', 'Hesarghatta Shyamasunder, Asha', 'Mathai, Sarah', 'Simon, Anna', 'Jha, Sujeet', 'Chowdry, Subhankar', 'Venkatesan, Radha', 'Raghupathy, Palany', 'Thomas, Nihal']
Journal Title : The Journal of clinical endocrinology and metabolism
Chapter : Section3
Journal Year : 2022
Cited by : 1.0

CONTEXT: Wolfram syndrome (WFS) is a rare autosomal recessive disorder characterized by juvenile-onset diabetes, diabetes insipidus, optic atrophy, deafness, and progressive neurodegeneration. However, due to the progressive nature of the disease and a la..... Read More

Keywords : ["geneassociate diabetes phenotype", "southern india", "founder mutation", "identification"]
PubMed Link : https://academic.oup.com/jcem/article-abstract/107/5/1328/6501334
Google Scholar Link : https://scholar.google.com/scholar?cites=18163151319108648388&as_sdt=5,31&sciodt=0,31&hl=en&num=20