Publication | Closed Access
Analysis of a Chinese pedigree with Zellweger syndrome reveals a novel PEX1 mutation by next-generation sequencing
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Citations
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References
2012
Year
Developmental BiologyMendelian DisorderGenetic DisorderNext-generation SequencingGeneticsNovel Pex1 MutationMolecular GeneticsDisease Gene IdentificationGenomicsMedicineChinese PedigreeVariant Interpretation
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