- Title
- Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome
- Creators
- Paulina Carmona-Mora - John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USACarolina A Encina - Centro de Estudios Científicos, CECS, Valdivia, ChileCesar P Canales - John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USALei Cao - John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USAJessica Molina - Centro de Estudios Científicos, CECS, Valdivia, ChilePamela Kairath - Centro de Estudios Científicos, CECS, Valdivia, ChileJuan I Young - John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USAKatherina Walz - John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USA
- Publication Details
- BMC molecular biology, Vol.11(1), pp.63-63
- Publisher
- BioMed Central
- Academic Unit
- Miller School of Medicine; John P. Hussman Institute for Human Genomics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
- Language
- English
- Resource Type
- Journal article
- PMID
- 20738874
- PMCID
- PMC2939504
- Record Identifier
- 991031558991702976
Journal article
Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome
BMC molecular biology, Vol.11(1), pp.63-63
2010-08-25
PMCID: PMC2939504
PMID: 20738874
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InCites Highlights
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- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.186 Chromosome Disorders
- 1.186.948 Digeorge Syndrome
- Web Of Science research areas
- Biochemistry & Molecular Biology
- ESI research areas
- Molecular Biology & Genetics
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Source: InCites