Associated Papers
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome.
Bitetto G et al.
Human Molecular Genetics, 2019
Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature.
Patt H et al.
Endocrine Connections, 2017
29180348 (PubMed )
Supplement: ec-6-901-t002.xls › Combined_Stat
Novel Mutations in a Patient with Triple A Syndrome.
Sanghvi J et al.
Indian Pediatrics, 2015
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