000 01311 a2200373 4500
005 20250513101452.0
264 0 _c19961203
008 199612s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/(SICI)1096-8628(19960202)61:4<356::AID-AJMG10>3.0.CO;2-R
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPegoraro, E
245 0 0 _aX-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cFeb 1996
300 _a356-62 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aDNA, Mitochondrial
650 0 4 _aDosage Compensation, Genetic
650 0 4 _aFemale
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aOptic Atrophies, Hereditary
_xdiagnosis
650 0 4 _aPedigree
700 1 _aCarelli, V
700 1 _aZeviani, M
700 1 _aCortelli, P
700 1 _aMontagna, P
700 1 _aBarboni, P
700 1 _aAngelini, C
700 1 _aHoffman, E P
773 0 _tAmerican journal of medical genetics
_gvol. 61
_gno. 4
_gp. 356-62
856 4 0 _uhttps://doi.org/10.1002/(SICI)1096-8628(19960202)61:4<356::AID-AJMG10>3.0.CO;2-R
_zAvailable from publisher's website
999 _c8828248
_d8828248