000 01420 a2200421 4500
005 20250516090452.0
264 0 _c20130219
008 201302s 0 0 eng d
022 _a0027-5107
024 7 _a10.1016/j.mrfmmm.2012.04.001
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTodorov, Tihomir
245 0 0 _aSpontaneous recurrent mutations and a complex rearrangement in the MECP2 gene in the light of current models of mutagenesis.
_h[electronic resource]
260 _bMutation research
_cJun 2012
300 _a69-72 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBase Sequence
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMethyl-CpG-Binding Protein 2
_xgenetics
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
650 0 4 _aRett Syndrome
_xgenetics
650 0 4 _aTranslocation, Genetic
700 1 _aTodorova, Albena
700 1 _aMotoescu, Cristina
700 1 _aDimova, Petia
700 1 _aIancu, Daniela
700 1 _aCraiu, Dana
700 1 _aStoian, Daniela
700 1 _aBarbarii, Ligia
700 1 _aBojinova, Veneta
700 1 _aMitev, Vanyo
773 0 _tMutation research
_gvol. 734
_gno. 1-2
_gp. 69-72
856 4 0 _uhttps://doi.org/10.1016/j.mrfmmm.2012.04.001
_zAvailable from publisher's website
999 _c21723870
_d21723870