000 01239 a2200373 4500
005 20250514043310.0
264 0 _c20030224
008 200302s 0 0 eng d
022 _a1381-3455
024 7 _a10.1076/apab.110.3.186.8294
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMaassen, J A
245 0 0 _aA case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness.
_h[electronic resource]
260 _bArchives of physiology and biochemistry
_cJul 2002
300 _a186-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aDNA, Mitochondrial
650 0 4 _aDeafness
_xgenetics
650 0 4 _aDiabetes Mellitus
_xgenetics
650 0 4 _aFemale
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aSyndrome
700 1 _aBiberoglu, S
700 1 _a't Hart, L M
700 1 _aBakker, E
700 1 _ade Knijff, P
773 0 _tArchives of physiology and biochemistry
_gvol. 110
_gno. 3
_gp. 186-8
856 4 0 _uhttps://doi.org/10.1076/apab.110.3.186.8294
_zAvailable from publisher's website
999 _c12101865
_d12101865