Clinical and mutational features of three Chinese children with congenital generalized lipodystrophy.
CONCLUSION: All of our patients exhibited characteristic features of CGL due to mutations in the BSCL2 gene.
PMID: 27612026 [PubMed - as supplied by publisher]
Source: JCRPE Journal of Clinical Research in Pediatric Endocrinology - Category: Endocrinology Tags: J Clin Res Pediatr Endocrinol Source Type: research
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