Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood - Concepedia

Concepedia

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Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood

120

Citations

23

References

2013

Year

Chihiro Ohba, Hitoshi Osaka, Mizue Iai, Sumimasa Yamashita, Yume Suzuki, Noriko Aida, Nobuyuki Shimozawa, Ayumi Takamura, Hiroshi Doi, Atsuko Katsumoto,

Developmental AnomalyRare DiseasesMendelian DisorderDiagnostic UtilityGenetic DisorderGeneticsDiagnosisWhole Exome SequencingDegenerative DiseaseNeurologyDisease Gene IdentificationNeuropathologyMedicine

References

	Year	Citations

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