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Updated: Jul 6, 2026
06:33
Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
Kunal Ray1, Moumita Chaki, Mainak Sengupta
1Indian Institute of Chemical Biology, Molecular and Human Genetics Division, 4, Raja S. C. Mullick Road, Jadavpur, 700 032, Kolkata, India. kunalray@gmail.com
Human Genetics
|April 3, 2008
Abstract
No abstract available in PubMed .
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