Mitochondrial DNA haplogroup 'R' is associated with Noonan syndrome of South India

Mitochondrion

Volumn 10, Issue 2, 2010, Pages 166-173

  Rani, Deepa Selvi ^a   Dhandapany, Perundurai S ^b,d   Nallari, Pratibha ^c   Govindaraj, Periyasamy ^a   Singh, Lalji ^a   Thangaraj, Kumarasamy ^a  

^a CENTRE FOR CELLULAR AND MOLECULAR BIOLOGY   (India)

^b MADURAI KAMARAJ UNIVERSITY   (India)

^c OSMANIA UNIVERSITY   (India)

^d MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

Congenital heart disease; Haplogroup; mtDNA; Noonan syndrome; PTPN11

Indexed keywords

MITOCHONDRIAL DNA; PROTEIN TYROSINE PHOSPHATASE SHP 2;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; INDIA; MALE; NOONAN SYNDROME; NUCLEOTIDE SEQUENCE; PHYLOGENY; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

AMINO ACID SUBSTITUTION; CLUSTER ANALYSIS; DNA, MITOCHONDRIAL; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; INDIA; MITOCHONDRIAL DISEASES; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NOONAN SYNDROME; PHYLOGENY; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY;

EID: 76049093263     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2009.12.146     Document Type: Article

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