B. Ploplis

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

A. Lalwani, J. Fex, J. R. Brister, 1994, American journal of human genetics.

Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.

S. Leal, G. Merlino, S. Riazuddin, 2009, American journal of human genetics.

Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

S. Riazuddin, Z. Ahmed, S. Riazuddin, 2004, BMC Medical Genetics.

Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3

K. Takeda, B. Ploplis, M. Tachibana, 1998, Nature Genetics.

The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat.

J. Fex, S. B. Potterf, M. Rivolta, 1992, Human molecular genetics.

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3.

F. Bess, E. Wilcox, M. Lesperance, 1995, Human molecular genetics.

Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

S. Riazuddin, S. Riazuddin, A. Griffith, 2001, Cell.