A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
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Genetics of Nonsyndromic Congenital Hearing LossHepatocyte Growth Factor-c-MET Signaling Mediates the Development of Nonsensory Structures of the Mammalian Cochlea and Hearing.Navigating genetic diagnostics in patients with hearing loss.Chromosomal microarray in a highly consanguineous population: diagnostic yield, utility of regions of homozygosity, and novel mutations.Genetic causes of moderate to severe hearing loss point to modifiers.Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.
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P2860
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
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2015 nî lūn-bûn
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2015年の論文
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name
A mutation of MET, encoding he ...... ith human DFNB97 hearing loss.
@ast
A mutation of MET, encoding he ...... ith human DFNB97 hearing loss.
@en
type
label
A mutation of MET, encoding he ...... ith human DFNB97 hearing loss.
@ast
A mutation of MET, encoding he ...... ith human DFNB97 hearing loss.
@en
prefLabel
A mutation of MET, encoding he ...... ith human DFNB97 hearing loss.
@ast
A mutation of MET, encoding he ...... ith human DFNB97 hearing loss.
@en
P2093
P2860
P1476
A mutation of MET, encoding he ...... with human DFNB97 hearing loss
@en
P2093
Ayesha Imtiaz
Ghulam Mujtaba
Julie M Schultz
Thomas B Friedman
P2860
P304
P356
10.1136/JMEDGENET-2015-103023
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P577
2015-05-04T00:00:00Z