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HUMU.22701
HUMU.22701
http://dx.doi.org/10.1002/HUMU.22701
Identification of pathogenic mechanisms of COCH mutations, abolished cochlin secretion, and intracellular aggregate formation: genotype-phenotype correlations in DFNA9 deafness and vestibular disorder.
P356
Q35216395-8CD8499C-680A-45BF-BA7E-021EB3DEEB7A
P356
HUMU.22701
http://dx.doi.org/10.1002/HUMU.22701