Steven J. H. Bom

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations

Kim Cryns, Markus Pfister, Ronald J. E. Pennings et al. · Human Genetics · 2002 · 90 citations · Full text

Wfs1 Gene, Genetic Disorder, Genetics +14

Progressive Cochleovestibular Impairment Caused by a Point Mutation in the <i>COCH</i> Gene at DFNA9

Steven J. H. Bom, Martijn H. Kemperman, Y.J.M. de Kok et al. · The Laryngoscope · 1999 · 48 citations

Vestibular Deterioration Precedes Hearing Deterioration in the P51S COCH Mutation (DFNA9): An Analysis in 74 Mutation Carriers

Anne M.L.C. Bischoff, P.L.M. Huygen, Martijn H. Kemperman et al. · Otology & Neurotology · 2005 · 46 citations

Speech Recognition Scores Related to Age and Degree of Hearing Impairment in DFNA2/KCNQ4 and DFNA9/COCH

Steven J. H. Bom, Els De Leenheer, F. X. Lemaire et al. · Archives of Otolaryngology - Head and Neck Surgery · 2001 · 42 citations

Progression of Low-Frequency Sensorineural Hearing Loss (DFNA6/14-WFS1)

Ronald J. E. Pennings, Steven J. H. Bom, Kim Cryns et al. · Archives of Otolaryngology - Head and Neck Surgery · 2003 · 42 citations