- Title: Subtitle
- Novel Mutations in BBS5 Highlight the Importance of This Gene in Non-Caucasian Bardet-Biedl Syndrome Patients
- Creators
- Tina Duelund Hjortshøj - Kennedy Center, Medical Genetics Laboratory, Glostrup, DenmarkKaren GRØNSKOV - Kennedy Center, Medical Genetics Laboratory, Glostrup, DenmarkAlisdair R PHILP - Department of Paediatrics, Howard Hughes Medical Institute, University of Iowa, Iowa City, Iowa, United StatesDarryl Y NISHIMURA - Department of Paediatrics, Howard Hughes Medical Institute, University of Iowa, Iowa City, Iowa, United StatesAdebowale ADEYEMO - National Human Genome Center, Howard University, Washington, District of Columbia, United StatesCharles N ROTIMI - National Human Genome Center, Howard University, Washington, District of Columbia, United StatesVal C SHEFFIELD - Department of Paediatrics, Howard Hughes Medical Institute, University of Iowa, Iowa City, Iowa, United StatesThomas ROSENBERG - Kennedy Center, National Eye Clinic, Hellerup, DenmarkKaren BRØNDUM-NIELSEN - Kennedy Center, Medical Genetics Laboratory, Glostrup, Denmark
- Resource Type
- Letter/Communication
- Publication Details
- American journal of medical genetics. Part A, Vol.146(4), pp.517-520
- Publisher
- Wiley-Liss; Hoboken, NJ
- DOI
- 10.1002/ajmg.a.32136
- PMID
- 18203199
- PMCID
- PMC2578871
- ISSN
- 1552-4825
- eISSN
- 1552-4833
- Language
- English
- Date published
- 2008
- Academic Unit
- Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Medical Genetics and Genomics; Ophthalmology and Visual Sciences
- Record Identifier
- 9984065485602771
Letter/Communication
Novel Mutations in BBS5 Highlight the Importance of This Gene in Non-Caucasian Bardet-Biedl Syndrome Patients
American journal of medical genetics. Part A, Vol.146(4), pp.517-520
2008
DOI: 10.1002/ajmg.a.32136
PMCID: PMC2578871
PMID: 18203199
Abstract
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