Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV. (Q40490300)

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Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV.
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    Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV. (English)
    Nathalie Verpoorten
    Kristl G Claeys
    Veerle Van Gerwen
    Willem Frans Arts
    Linda De Meirleir
    Kathelijn Keymolen
    Chantal Ceuterick-de Groote
    Peter De Jonghe
    Vincent Timmerman

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