GJB2 MUTATIONS IN BALUCHI POPULATION

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NAGHAVI A.; NISHIMURA C.; KAHRIZI K.

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Journal Paper

Paper Information

Journal: JOURNAL OF GENETICS Year:2008 | Volume:87 | Issue:2 Page(s): 195-197

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Information Journal Paper

Title

GJB2 MUTATIONS IN BALUCHI POPULATION

Author(s)

NAGHAVI A. | NISHIMURA C. | KAHRIZI K. | Issue Writer Certificate

Keywords

Not Registered.

Abstract

Cites

A NOVEL COMPOUND HETEROZYGOUS MUTATION (35DELG, 363DELC) IN THE CONNEXIN 26 GENE CAUSES NON-SYNDROMIC AUTOSOMAL RECESSIVE HEARING LOSS (CASE REPORT)
INVESTIGATION OF CONNEXIN 26 MUTATIONS AND THREE LARGE DELETIONS SPANNING CONNEXIN 30 IN 63 IRANIAN FAMILIES WITH AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING LOSS

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APA: Copy

NAGHAVI, A., NISHIMURA, C., & KAHRIZI, K.. (2008). GJB2 MUTATIONS IN BALUCHI POPULATION. JOURNAL OF GENETICS, 87(2), 195-197. SID. https://sid.ir/paper/578348/en

Vancouver: Copy

NAGHAVI A., NISHIMURA C., KAHRIZI K.. GJB2 MUTATIONS IN BALUCHI POPULATION. JOURNAL OF GENETICS[Internet]. 2008;87(2):195-197. Available from: https://sid.ir/paper/578348/en

IEEE: Copy

A. NAGHAVI, C. NISHIMURA, and K. KAHRIZI, “GJB2 MUTATIONS IN BALUCHI POPULATION,” JOURNAL OF GENETICS, vol. 87, no. 2, pp. 195–197, 2008, [Online]. Available: https://sid.ir/paper/578348/en

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