Concepedia

Publication | Open Access

Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

DOIFull Paper Access

71

Citations

32

References

2010

Year

Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, P.L.M. Huygen, Ghazanfar Ali, Lies H. Hoefsloot, Joris A. Veltman, Frans P.M. Cremers, Sulman Basit, Muhammad Ansar,
The American Journal of Human Genetics

References

YearCitations

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