000 01427 a2200445 4500
005 20250515055946.0
264 0 _c20070614
008 200706s 0 0 eng d
022 _a0009-9163
024 7 _a10.1111/j.1399-0004.2007.00763.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCho, H-J
245 0 0 _aMitochondrial GTPase mitofusin 2 mutations in Korean patients with Charcot-Marie-Tooth neuropathy type 2.
_h[electronic resource]
260 _bClinical genetics
_cMar 2007
300 _a267-72 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAsian People
650 0 4 _aBase Sequence
650 0 4 _aCharcot-Marie-Tooth Disease
_xdiagnosis
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aGTP Phosphohydrolases
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMembrane Proteins
_xgenetics
650 0 4 _aMitochondrial Proteins
_xgenetics
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
650 0 4 _aPedigree
700 1 _aSung, D H
700 1 _aKim, B J
700 1 _aKi, C-S
773 0 _tClinical genetics
_gvol. 71
_gno. 3
_gp. 267-72
856 4 0 _uhttps://doi.org/10.1111/j.1399-0004.2007.00763.x
_zAvailable from publisher's website
999 _c16868571
_d16868571