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Q34184437-4EB60C06-970C-4C1D-8B55-6C74404C2710
Q34184437-4EB60C06-970C-4C1D-8B55-6C74404C2710
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Statement
http://www.wikidata.org/entity/statement/Q34184437-4EB60C06-970C-4C1D-8B55-6C74404C2710
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment.
P2860
Q34184437-4EB60C06-970C-4C1D-8B55-6C74404C2710
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34184437-4EB60C06-970C-4C1D-8B55-6C74404C2710
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Statement
wasDerivedFrom
94bb7ec023b75ba98335e0e6030032f012f1f53c
P2860
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family