Alström syndrome: intrafamilial phenotypic variability in sibs with a novel nonsense mutation of the ALMS1 gene
- 29 January 2004
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 65 (2) , 156-157
- https://doi.org/10.1111/j.0009-9163.2004.00204.x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndromeNature Genetics, 2002
- Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional familiesAmerican Journal of Medical Genetics, 1997
- Natural history of Alström syndrome in early childhood: Onset with dilated cardiomyopathyThe Journal of Pediatrics, 1996
- Late onset dilated cardiomyopathy in a unique familial syndrome of hypogonadism and metabolic abnormalitiesAmerican Heart Journal, 1987