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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Query Trace: Syndrome and BSCL2[original query]
Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient.
Iranian biomedical journal 2016 Jul .
Alaei Mohammad Reza, Talebi Saeed, Ghofrani Mohammad, Taghizadeh Mohsen, Keramatipour Mohamm
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