Unraveling of Enigmatic Hearing-Impaired GJB2 Single Heterozygotes by Massive Parallel Sequencing: DFNB1 or Not?
about
Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic intervention.Human diseases associated with connexin mutations.The genetic dissection of Myo7a gene expression in the retinas of BXD mice.
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Unraveling of Enigmatic Hearing-Impaired GJB2 Single Heterozygotes by Massive Parallel Sequencing: DFNB1 or Not?
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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 April 2016
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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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Unraveling of Enigmatic Hearin ...... llel Sequencing: DFNB1 or Not?
@en
Unraveling of Enigmatic Hearin ...... llel Sequencing: DFNB1 or Not?
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Unraveling of Enigmatic Hearin ...... llel Sequencing: DFNB1 or Not?
@en
Unraveling of Enigmatic Hearin ...... llel Sequencing: DFNB1 or Not?
@nl
prefLabel
Unraveling of Enigmatic Hearin ...... llel Sequencing: DFNB1 or Not?
@en
Unraveling of Enigmatic Hearin ...... llel Sequencing: DFNB1 or Not?
@nl
P2093
P2860
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P1476
Unraveling of Enigmatic Hearin ...... llel Sequencing: DFNB1 or Not?
@en
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Ah Reum Kim
Byung Yoon Choi
Eun-Hee Jeon
Min Young Kim
Nayoung K D Kim
So Young Kim
P2860
P356
10.1097/MD.0000000000003029
P407
P577
2016-04-01T00:00:00Z