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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
8
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pubmed:dateCreated |
2009-8-6
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pubmed:abstractText |
Maternally inherited diabetes and deafness (MIDD) is a rare form of diabetes with a matrilineal transmission, sensorineural hearing loss, and macular pattern dystrophy due to an A to G transition at position 3243 of mitochondrial DNA (mtDNA) (m.3243A>G). The phenotypic heterogeneity of MIDD may be the consequence of different levels of mutated mtDNA among mitochondria in a given tissue.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1945-7197
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pubmed:author |
pubmed-author:AmbonvilleCC,
pubmed-author:BauduceauBB,
pubmed-author:BeaufilsSS,
pubmed-author:Bellanné-ChantelotCC,
pubmed-author:BernardLL,
pubmed-author:BertilGG,
pubmed-author:BlickleJ-FJF,
pubmed-author:BouhanickBB,
pubmed-author:Cahen-VarsauxJJ,
pubmed-author:CaillebaAA,
pubmed-author:CasanovaSS,
pubmed-author:CathebrasPP,
pubmed-author:CharpentierGG,
pubmed-author:ChedinPP,
pubmed-author:CreaTT,
pubmed-author:DelemerBB,
pubmed-author:Dubois-LaforgueDD,
pubmed-author:DucheminFF,
pubmed-author:DucluzeauP HPH,
pubmed-author:DusselierLL,
pubmed-author:GabreauTT,
pubmed-author:GinHH,
pubmed-author:GrimaldiAA,
pubmed-author:GuerciBB,
pubmed-author:GuillausseauP JPJ,
pubmed-author:JacquinVV,
pubmed-author:KaloustianEE,
pubmed-author:Laloi-MichelinMM,
pubmed-author:LargerEE,
pubmed-author:Lecleire-ColletAA,
pubmed-author:LorenziniFF,
pubmed-author:LouisJJ,
pubmed-author:MassinPP,
pubmed-author:MaussetJJ,
pubmed-author:MeasTT,
pubmed-author:Mitochondrial Diabetes French Study Group,
pubmed-author:MuratAA,
pubmed-author:Nadler-FluteauSS,
pubmed-author:OlivierFF,
pubmed-author:Paquis-FlucklingerVV,
pubmed-author:Paris-BockelDD,
pubmed-author:RaynaudII,
pubmed-author:ReznikYY,
pubmed-author:RivelineJ PJP,
pubmed-author:SchneebeliSS,
pubmed-author:Sola-GazagnesAA,
pubmed-author:SonnetEE,
pubmed-author:ThomasJ LJL,
pubmed-author:TimsitJJ,
pubmed-author:TrabulsiBB,
pubmed-author:VialettesBB,
pubmed-author:VirallyMM
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pubmed:issnType |
Electronic
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pubmed:volume |
94
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3025-30
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pubmed:meshHeading |
pubmed-meshheading:19470619-Adult,
pubmed-meshheading:19470619-Age Factors,
pubmed-meshheading:19470619-Body Mass Index,
pubmed-meshheading:19470619-DNA, Mitochondrial,
pubmed-meshheading:19470619-Deafness,
pubmed-meshheading:19470619-Diabetes Mellitus,
pubmed-meshheading:19470619-Female,
pubmed-meshheading:19470619-Hemoglobin A, Glycosylated,
pubmed-meshheading:19470619-Humans,
pubmed-meshheading:19470619-Leukocytes,
pubmed-meshheading:19470619-Male,
pubmed-meshheading:19470619-Middle Aged,
pubmed-meshheading:19470619-Mitochondrial Diseases,
pubmed-meshheading:19470619-Point Mutation,
pubmed-meshheading:19470619-Prospective Studies,
pubmed-meshheading:19470619-Sex Characteristics
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pubmed:year |
2009
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pubmed:articleTitle |
The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.
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pubmed:affiliation |
Department of Internal Medicine B, Hôpital Lariboisière, 2 Rue Ambroise Paré, Paris Cedex 10, France.
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pubmed:publicationType |
Journal Article,
Multicenter Study
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