ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits
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Alström syndrome (AS) is characterised by metabolic deficits, retinal dystrophy, sensorineural hearing loss, dilated cardiomyopathy and multi-organ fibrosis. Elucidating the function of the mutated gene, ALMS1, is critical for the development of specific trea... ...
