Concepedia

A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family

Chuan Yu, Xiangming Meng, Shanfang Zhang, Guoping Zhao, Landian Hu, Xiangyin Kong

Genomics · 2003 · 82 citations · 4 references

DOI

Concepts

References

4

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Lut Van Laer, E. H. Huizing, Margriet Verstreken et al. · Nature Genetics · 1998 · 391 citations · Full text

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Mutation in Transcription Factor <i>POU4F3</i> Associated with Inherited Progressive Hearing Loss in Humans

Oz Vahava, Robert J. Morell, Eric D. Lynch et al. · Science · 1998 · 350 citations

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A Follow-Up Study in a Family with Dominant Progressive Inner Ear Deafness

E. H. Huizing, W. S.I.M. van den Wijngaart, J. Verschuure · Acta Oto-Laryngologica · 1983 · 27 citations

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Follow-Up Study in a Family with Dominant Progressive Hereditary Sensorineural Hearing Impairment I. Analysis of Hearing Deterioration

W. S.I.M. van den Wijngaart, J. Verschuure, M. P. Brocaar et al. · International Journal of Audiology · 1985 · 23 citations

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