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The molecular genetics of Bardet-Biedl syndrome
- Source :
- Current opinion in geneticsdevelopment. 11(3)
- Publication Year :
- 2001
-
Abstract
- Bardet-Biedl syndrome (BBS) has been shown to be a genetically heterogeneous disorder involving genes mapping to at least six known loci. One BBS gene (MKKS) has been identified and the form of the disorder caused by this gene is allelic to McKusick-Kaufman syndrome. MKKS codes for a putative chaperonin, suggesting that other BBS genes may also code for components of chaperone complexes or be substrates of chaperone function.
- Subjects :
- congenital, hereditary, and neonatal diseases and abnormalities
medicine.medical_specialty
Chaperonins
Ubiquitin-Protein Ligases
Group II Chaperonins
Biology
T-Complex Genome Region
MKKS
McKusick–Kaufman syndrome
Bardet–Biedl syndrome
Molecular genetics
Genetics
medicine
Animals
Humans
Cloning, Molecular
Gene
Bardet-Biedl Syndrome
t-Complex Genome Region
Polydactyly
Genetic heterogeneity
fungi
Intracellular Signaling Peptides and Proteins
Chromosome Mapping
Nuclear Proteins
medicine.disease
Microtubule-Associated Proteins
Developmental Biology
Molecular Chaperones
Subjects
Details
- ISSN :
- 0959437X
- Volume :
- 11
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Current opinion in geneticsdevelopment
- Accession number :
- edsair.doi.dedup.....485c42f3814acc6b8a4a4dc1df1631eb