Familial primary pulmonary hypertension (Gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene

American Journal of Human Genetics

Volumn 67, Issue 3, 2000, Pages 737-744

  Deng, Zemin ^a,b   Morse, Jane H ^b   Slager, Susan L ^a   Cuervo, Nieves ^a   Moore, Keith J ^a   Venetos, George ^b   Kalachikov, Sergey ^d   Cayanis, Eftihia ^d   Fischer, Stuart G ^d   Barst, Robyn J ^c   Hodge, Susan E ^a,e   Knowles, James A ^a,d,f  

^a NEW YORK STATE PSYCHIATRIC INSTITUTE   (United States)

^b Departments of Medicine   (United States)

^c Departments of Pediatrics   (United States)

^d New York Presbyterian Columbia University Medical Center   (United States)

^e Columbia University ^*  (United States)

^f Taub Institute for Research on Alzheimer s Disease and the Aging Brain   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN RECEPTOR; FENFLURAMINE; MICROSATELLITE DNA; PHENTERMINE;

ARTERIOLE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL PROLIFERATION; CHROMOSOME 2Q; CHROMOSOME MAP; FAMILIAL DISEASE; GENE MAPPING; GENE MUTATION; GENOTYPE; HAPLOTYPE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PREDICTION; PRIORITY JOURNAL; PULMONARY HYPERTENSION; SIGNAL TRANSDUCTION;

EID: 0033838125     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/303059     Document Type: Article

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