Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in two cases of sensorimotor neuropathy and one case of motor neuropathy
about
Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in two cases of sensorimotor neuropathy and one case of motor neuropathy
description
article
@en
im August 2018 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2018
@uk
name
Novel mutations in HINT1 gene ...... d one case of motor neuropathy
@en
Novel mutations in HINT1 gene ...... d one case of motor neuropathy
@nl
type
label
Novel mutations in HINT1 gene ...... d one case of motor neuropathy
@en
Novel mutations in HINT1 gene ...... d one case of motor neuropathy
@nl
prefLabel
Novel mutations in HINT1 gene ...... d one case of motor neuropathy
@en
Novel mutations in HINT1 gene ...... d one case of motor neuropathy
@nl
P2093
P1476
Novel mutations in HINT1 gene ...... d one case of motor neuropathy
@en
P2093
P304
P356
10.1016/J.NMD.2018.05.003
P407
P577
2018-05-15T00:00:00Z