Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type - Concepedia

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Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type

DOI Full Paper Access

61

Citations

20

References

2011

Year

Byung-Joo Min, Namshin Kim, Taesu Chung, Ok-Hwa Kim, Gen Nishimura, Chin Youb Chung, Hae Ryong Song, Hyun Woo Kim, Hyeran Lee, Jiwoong Kim,

The American Journal of Human Genetics

Joint LaxityMendelian DisorderSpondyloepimetaphyseal DysplasiaGenetic DisorderMedicineGeneticsPathologyLeptodactylic TypeMolecular GeneticsDisease Gene IdentificationGenomicsMolecular DiagnosticsVariant Interpretation

References

	Year	Citations

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