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Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière's Disease.

Zohreh MehrjooKimia KahriziMarzieh MohseniMojdeh AkbariSanaz ArzhangiKhadijeh JalalvandHossein NajmabadiMohammad FarhadiMohammad MohseniAlimohamad AsghariSaleh MohebbiAhmad Daneshi
Published in: Archives of Iranian medicine (2020)
The phenotype observed in the proband described here, i.e. vertigo, poor sense of smell, tinnitus, and borderline hearing ability, may originate from aberrant changes in the cerebellum and limbic system due to a deleterious mutation in the LSAMP gene; hence, LSAMP mutation is a possible candidate for the etiology of MD in this family.
Keyphrases
  • genome wide
  • genome wide analysis
  • transition metal