Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency☆
Non-synonymous mutations affecting both alleles of PCSK1 (proprotein convertase 1/3) are associated with obesity and impaired prohormone processing. We report a proband who was compound heterozygous for a maternally inherited frameshift mutation and a paternally inherited 474kb deletion that encompa...
Main Authors: | , , , , , , , , |
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Format: | Online |
Language: | English |
Published: |
Academic Press
2013
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759845/ |