Mutation study of Spanish patients with Hereditary Hemorrhagic Telangiectasia

BMC Medical Genetics

Volumn 9, Issue , 2008, Pages

  Fontalba, Ana ^b   Fernandez L, Africa ^a,d   García Alegria, Eva ^b   Albiñana, Virginia ^a,d   Garrido Martin, Eva M ^a,d   Blanco, Francisco J ^a,d   Zarrabeitia, Roberto ^c,d   Perez Molino, Alfonso ^c,d   Bernabeu Herrero, Maria E ^a   Ojeda, Maria Luisa ^a,d   Fernandez Luna, Jose L ^b   Bernabeu, Carmelo ^a,d   Botella, Luisa M ^a,d  

^a CENTRO DE INVESTIGACIONES BIOLÓGICAS   (Spain)

^b HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

^c HOSPITAL SIERRALLANA   (Spain)

^d INSTITUTO DE SALUD CARLOS III   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN RECEPTOR LIKE KINASE 1; ENDOGLIN; PHOSPHOTRANSFERASE; ACTIVIN RECEPTOR 2; ACVRL1 PROTEIN, HUMAN; CELL SURFACE RECEPTOR; ENG PROTEIN, HUMAN; LEUKOCYTE ANTIGEN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CONTROLLED STUDY; FAMILY STUDY; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PULMONARY ARTERIOVENOUS FISTULA; RENDU OSLER WEBER DISEASE; SPAIN; SYMPTOM; VASCULAR DISEASE; EXON; GENETICS; MUTATION; PEDIGREE;

ACTIVIN RECEPTORS, TYPE II; ANTIGENS, CD; EXONS; HUMANS; MUTATION; MUTATION, MISSENSE; PEDIGREE; RECEPTORS, CELL SURFACE; SPAIN; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

EID: 49849089070     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-9-75     Document Type: Article

References (35)

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