Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

Authors

Leopoldo Zelante

Published

September 1, 1997

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Journal

Human Molecular Genetics

Topics

Endocrine And Autonomic Systems

DOI

10.1093/hmg/6.9.1605

Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

Authors

Leopoldo Zelante

Published

September 1, 1997

Add a comment...

Supporters

Support the authors with ResearchCoin

Journal

Human Molecular Genetics

Topics

Endocrine And Autonomic Systems

DOI

10.1093/hmg/6.9.1605

Paper

Paper

Paper

Paper

Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

Supporters

Journal

Topics

DOI

Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

Supporters

Journal

Topics

DOI