Genetic basis of olfactory deficits

Idan Menashe, Ester Feldmesser, Doron Lancet

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

1 Scopus citations

Abstract

The completion of the human genome sequencing has opened new opportunities to better understand complex biological systems. In this realm, the human sense of smell is an excellent example of how genome analysis provides new information on genome organization and on deficits. Before the advent of genomic tools, the understanding of this highly sophisticated sensory neuronal pathway has been rather sketchy. In this chapter we summarize the relevant progress made in the last decade, and highlight the initial elucidation of two classes of olfactory deficits and their possible underlying genetic mechanisms.

Original languageEnglish GB
Title of host publicationGenomic Disorders
Subtitle of host publicationThe Genomic Basis of Disease
PublisherHumana Press
Pages101-113
Number of pages13
ISBN (Print)1588295591, 9781588295590
DOIs
StatePublished - 1 Dec 2006
Externally publishedYes

ASJC Scopus subject areas

  • Medicine (all)

Fingerprint

Dive into the research topics of 'Genetic basis of olfactory deficits'. Together they form a unique fingerprint.

Cite this