Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome
- 8 April 2002
- journal article
- letter
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 31 (1), 74-78
- https://doi.org/10.1038/ng867
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndromeNature Genetics, 2002
- Obesity as a medical problemNature, 2000
- Alström syndrome: further evidence for linkage to human chromosome 2p13Human Genetics, 1999
- Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African familyHuman Genetics, 1998
- Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional familiesAmerican Journal of Medical Genetics, 1997
- Homozygosity Mapping of Alstrom Syndrome to Chromosome 2pHuman Molecular Genetics, 1997
- Natural history of Alström syndrome in early childhood: Onset with dilated cardiomyopathyThe Journal of Pediatrics, 1996
- Hepatic dysfunction in Alström diseaseAmerican Journal of Medical Genetics, 1991
- Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction.Journal of Medical Genetics, 1990
- REPORT OF THREE CASES WITH FURTHER DELINEATION OF THE CLINICAL, PATHOPHYSIOLOGICAL, AND GENETIC ASPECTS FO THE DISORDERMedicine, 1973