Dawson C

No ORCID on file · 1 paper in corpus · active 2020
2020
Orphanet journal of rare diseases ·doi:10.1186/s13023-020-01468-8

Alström Syndrome (ALMS) is an ultra-rare multisystem genetic disorder caused by autosomal recessive variants in the ALMS1 gene, which is located on chromosome 2p13. ALMS is a multisystem, progressive disease characterised by visual disturba…