A novel homozygous mutation in the EC1/EC2 interaction domain of the gap junction complex connexon 26 leads to profound hearing impairment
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A novel homozygous mutation in the EC1/EC2 interaction domain of the gap junction complex connexon 26 leads to profound hearing impairment
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 16 January 2014
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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A novel homozygous mutation in ...... to profound hearing impairment
@en
A novel homozygous mutation in ...... o profound hearing impairment.
@nl
type
label
A novel homozygous mutation in ...... to profound hearing impairment
@en
A novel homozygous mutation in ...... o profound hearing impairment.
@nl
prefLabel
A novel homozygous mutation in ...... to profound hearing impairment
@en
A novel homozygous mutation in ...... o profound hearing impairment.
@nl
P2093
P2860
P356
P1476
A novel homozygous mutation in ...... to profound hearing impairment
@en
P2093
Antje Aschendorff
Nicola Prera
Ralf Birkenhäger
Roland Laszig
P2860
P304
P356
10.1155/2014/307976
P407
P50
P577
2014-01-16T00:00:00Z