Gerard W. Hensels

The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A

Linda J. Valentijn, Pieter A. Bolhuis, Ina Zorn et al. · Nature Genetics · 1992 · 317 citations

Genetics, Experimental Neuropathology, Pathology +5

Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot–Marie–Tooth disease type 1B

Tanja Kulkens, Pieter A. Bolhuis, Ruud A. Wolterman et al. · Nature Genetics · 1993 · 184 citations

Neurodegenerative Diseases, Genetic Disorder, Genetics +7

De-novo mutation in hereditary motor and sensory neuropathy type I

Jessica E. Hoogendijk, Gerard W. Hensels, Emiel A. M. Janssen et al. · The Lancet · 1992 · 161 citations

Rare Diseases, Hereditary Motor, Mendelian Disorder +10

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

Pieter A. Bolhuis, Gerard W. Hensels, Theo J.M. Hulsebos et al. · PubMed · 1991 · 143 citations

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)

Emiel A. M. Janssen, Stephan Kemp, Gerard W. Hensels et al. · Human Genetics · 1997 · 58 citations · Full text

Mendelian Disorder, Connexin32 Gene Mutations, Medicine +7