Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37
COL11A1基因剪接变异是导致非综合征性听力损失DFNA37的原因
期刊:Genetics in Medicine
影响因子:6.2
doi:10.1038/s41436-018-0285-0
Booth, Kevin T; Askew, James W; Talebizadeh, Zohreh; Huygen, Patrick L M; Eudy, James; Kenyon, Judith; Hoover, Denise; Hildebrand, Michael S; Smith, Katherine R; Bahlo, Melanie; Kimberling, William J; Smith, Richard J H; Azaiez, Hela; Smith, Shelley D