FUNCTIONAL ANALYSIS OF HUMAN CX26 MUTATIONS ASSOCIATED WITH DEAFNESS

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WHITE T.W.

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Journal Paper

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Journal: BRAIN RESEARCH REVIEW Year:2000 | Volume:32 | Issue:- Page(s): 181-183

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Information Journal Paper

Title

FUNCTIONAL ANALYSIS OF HUMAN CX26 MUTATIONS ASSOCIATED WITH DEAFNESS

Author(s)

WHITE T.W. | Issue Writer Certificate

Keywords

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Abstract

Cites

A NOVEL COMPOUND HETEROZYGOUS MUTATION (35DELG, 363DELC) IN THE CONNEXIN 26 GENE CAUSES NON-SYNDROMIC AUTOSOMAL RECESSIVE HEARING LOSS (CASE REPORT)
FREQUENCY OF A VERY RARE 35DELG MUTATION IN TWO ETHNIC GROUPS OF IRANIAN POPULATIONS

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APA: Copy

WHITE, T.W.. (2000). FUNCTIONAL ANALYSIS OF HUMAN CX26 MUTATIONS ASSOCIATED WITH DEAFNESS. BRAIN RESEARCH REVIEW, 32(-), 181-183. SID. https://sid.ir/paper/533043/en

Vancouver: Copy

WHITE T.W.. FUNCTIONAL ANALYSIS OF HUMAN CX26 MUTATIONS ASSOCIATED WITH DEAFNESS. BRAIN RESEARCH REVIEW[Internet]. 2000;32(-):181-183. Available from: https://sid.ir/paper/533043/en

IEEE: Copy

T.W. WHITE, “FUNCTIONAL ANALYSIS OF HUMAN CX26 MUTATIONS ASSOCIATED WITH DEAFNESS,” BRAIN RESEARCH REVIEW, vol. 32, no. -, pp. 181–183, 2000, [Online]. Available: https://sid.ir/paper/533043/en

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