000 01533 a2200421 4500
005 20250516134829.0
264 0 _c20130621
008 201306s 0 0 eng d
022 _a1471-2431
024 7 _a10.1186/1471-2431-13-27
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aObara-Moszynska, Monika
245 0 0 _aA novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment.
_h[electronic resource]
260 _bBMC pediatrics
_cFeb 2013
300 _a27 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAtrioventricular Block
_xdiagnosis
650 0 4 _aBase Sequence
650 0 4 _aCardiomyopathy, Dilated
_xdiagnosis
650 0 4 _aDNA, Mitochondrial
650 0 4 _aFatal Outcome
650 0 4 _aGrowth Disorders
_xdrug therapy
650 0 4 _aHuman Growth Hormone
_xdeficiency
650 0 4 _aHumans
650 0 4 _aKearns-Sayre Syndrome
_xcomplications
650 0 4 _aMale
650 0 4 _aRecombinant Proteins
650 0 4 _aSequence Deletion
700 1 _aMaceluch, Jaroslaw
700 1 _aBobkowski, Waldemar
700 1 _aBaszko, Artur
700 1 _aJaremba, Oskar
700 1 _aKrawczynski, Maciej R
700 1 _aNiedziela, Marek
773 0 _tBMC pediatrics
_gvol. 13
_gp. 27
856 4 0 _uhttps://doi.org/10.1186/1471-2431-13-27
_zAvailable from publisher's website
999 _c22516364
_d22516364