Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families

Collegium Antropologicum

Volumn 30, Issue 1, 2006, Pages 171-174

  Martin Kleiner, Irena ^a   Gabrilovac, Jelka ^a   Bradvica, Mario ^b   Vidović, Tomislav ^c,e   Cerovski, Branimir ^c,e   Fumić, Ksenija ^d,e   Boranić, Milivoj ^a  

^a RUDER BO KOVI INSTITUTE   (Croatia)

^b UNIVERSITY HOSPITAL OSIJEK   (Croatia)

^c UNIVERSITY OF ZAGREB   (Croatia)

^d UNIVERSITY OF ZAGREB   (Croatia)

^e KBC Zagreb   (Croatia)

Author keywords

G11778A point mutation; LHON; Mitochondrial DNA; Visual impairment

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; CHILD; CONFERENCE PAPER; CROATIA; FAMILY; FEMALE; GENETICS; HETEROZYGOTE; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; MIDDLE AGED; MOLECULAR BIOLOGY; PEDIGREE; POINT MUTATION;

ADULT; CHILD; CROATIA; DNA, MITOCHONDRIAL; FAMILY; FEMALE; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MOLECULAR BIOLOGY; OPTIC ATROPHY, HEREDITARY, LEBER; PEDIGREE; POINT MUTATION;

EID: 33645691818     PISSN: 03506134     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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