A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [10]

A. K. Lalwani; W. M. Luxford; A. N. Mhatre; A. Attaie; E. R. Wilcox; C. M. Castelein

doi:10.1086/302216

A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [10]

A. K. Lalwani, W. M. Luxford, A. N. Mhatre, A. Attaie, E. R. Wilcox, C. M. Castelein

Research output: Contribution to journal › Letter › peer-review

32 Scopus citations

Original language	English
Pages (from-to)	318-323
Number of pages	6
Journal	American Journal of Human Genetics
Volume	64
Issue number	1
DOIs	https://doi.org/10.1086/302216
State	Published - 1999
Externally published	Yes

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10.1086/302216

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@article{51c243e257954cf383665418ff2fd0a4,

title = "A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [10]",

author = "Lalwani, {A. K.} and Luxford, {W. M.} and Mhatre, {A. N.} and A. Attaie and Wilcox, {E. R.} and Castelein, {C. M.}",

note = "Funding Information: We thank the family who made this research possible. We express our deepest appreciation to Drs. Fred Linthicum and Jean Moore, of the House Ear Institute, for their unselfish contributions. Finally, we acknowledge Michael Ng for his efforts in the initial screening of this family. This study was supported in part by National Institute on Deafness and Other Communication Disorders (National Institutes of Health) grants K08 DC 00112 (to A.K.L.) and DC00026 (to E.R.W.); the American Hearing Research Foundation; the National Organization for Hearing Research; the Deafness Research Foundation; Hearing Research, Inc.; and the REAC Jacobsen Fund, School of Medicine, University of California, San Francisco. C.M.C. was supported by grants from the Deafness Research Foundation, the Genentech Foundation, and the School of Medicine, University of California, San Francisco. ",

year = "1999",

doi = "10.1086/302216",

language = "English",

volume = "64",

pages = "318--323",

journal = "American Journal of Human Genetics",

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T1 - A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [10]

AU - Lalwani, A. K.

AU - Luxford, W. M.

AU - Mhatre, A. N.

AU - Attaie, A.

AU - Wilcox, E. R.

AU - Castelein, C. M.

N1 - Funding Information: We thank the family who made this research possible. We express our deepest appreciation to Drs. Fred Linthicum and Jean Moore, of the House Ear Institute, for their unselfish contributions. Finally, we acknowledge Michael Ng for his efforts in the initial screening of this family. This study was supported in part by National Institute on Deafness and Other Communication Disorders (National Institutes of Health) grants K08 DC 00112 (to A.K.L.) and DC00026 (to E.R.W.); the American Hearing Research Foundation; the National Organization for Hearing Research; the Deafness Research Foundation; Hearing Research, Inc.; and the REAC Jacobsen Fund, School of Medicine, University of California, San Francisco. C.M.C. was supported by grants from the Deafness Research Foundation, the Genentech Foundation, and the School of Medicine, University of California, San Francisco.

PY - 1999

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U2 - 10.1086/302216

DO - 10.1086/302216

M3 - Letter

C2 - 9915977

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