Medicina Genómica de México,
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37 #openaccess https://goo.gl/1nvHEQ
Genética Médica Querétaro,
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37 #openaccess https://goo.gl/1nvHEQ
ACMG - American College of Medical Genetics and Genomics,
Study aimed at determining the genetic cause of autosomal dominant nonsyndromic hearing loss segregating in a multigenerational…
Genetics in Medicine,
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37 #openaccess https://goo.gl/1nvHEQ