(Q73245087)

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A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female

scientific article published on 01 September 1999

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Europe PubMed Central

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10586279

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A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female (English)

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10586279

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2 November 2019

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Lin GS

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10586279

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Glass JD

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10586279

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Shumas S

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10586279

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2 November 2019

Scherer SS

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10586279

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Fischbeck KH

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10586279

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1 September 1999

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10586279

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2 November 2019

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Annals of the New York Academy of Sciences

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10586279

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883

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page(s)

481-484

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(Q73245087)

A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female

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