Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans (Q48045551)
scientific article published in September 1997
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Current Data About Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
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(P1476) "Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans" (language: en)
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(P2093) L Zelante
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P Gasparini
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L D'Agruma
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N Govea
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M Milá
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M D Monica
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J Lutfi
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M Shohat
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E Mansfield
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K Delgrosso
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E Rappaport
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S Surrey
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P Fortina
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other details
description scientific article published in September 1997

External Links
(P356) 10.1093/HMG/6.9.1605
(P698) 9285800
(P5875) 277549233