De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness - Concepedia

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De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness

DOI Full Paper Access

48

Citations

39

References

2018

Year

Isabelle Schrauwen, Elina Kari, Jacob Mattox, Lorida Llaci, Joanna Smeeton, Marcus Naymik, David W. Raible, James A. Knowles, J. Gage Crump, Matthew J. Huentelman,

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiologyNeurotologyDisease Gene IdentificationArtsMedicineAuditory SystemHearing Loss

References

	Year	Citations

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