Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness [4]

T. Ben-Yosef, M. Wattenhofer, S. Riazuddin, Z. M. Ahmed, H. S. Scott, J. Kudoh, K. Shibuya, S. E. Antonarakis, B. Bonne-Tamir, U. Radhakrishna, S. Naz, Z. Ahmed, S. Riazuddin, A. Pandya, W. E. Nance, E. R. Wilcox, T. B. Friedman*, R. J. Morell

*Corresponding author for this work

Research output: Contribution to journalLetterpeer-review

52 Scopus citations
Original languageEnglish
Pages (from-to)396-400
Number of pages5
JournalJournal of Medical Genetics
Volume38
Issue number6
DOIs
StatePublished - 2001
Externally publishedYes

Funding

FundersFunder number
National Institute on Deafness and Other Communication DisordersZ01DC000035

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