A family with Von Hippel-Lindau disease revealed by pheochromocytoma

Hypertension Research

Volumn 24, Issue 4, 2001, Pages 445-450

  Tomita, N ^a   Moriguchi, A ^a   Yamasaki, K ^a   Taniyama, Y ^a   Kotani, N ^a   Hashiya, N ^a   Yoshida, M ^a   Yao, M ^a   Higaki, J ^a   Ogihara, T ^a  

^a OSAKA UNIVERSITY HOSPITAL   (Japan)

Author keywords

Missense mutation; Pheochromocytoma; Von Hippel Lindau disease

Indexed keywords

ADENINE; GUANINE; NUCLEOTIDE;

ADULT; ANGIOMA; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE PREDISPOSITION; FAMILY; FEMALE; GENETIC ANALYSIS; GERM LINE; HEMANGIOBLASTOMA; HUMAN; KIDNEY CARCINOMA; MALE; MISSENSE MUTATION; NEOPLASM; NUCLEIC ACID BASE SUBSTITUTION; PANCREAS CYST; PHEOCHROMOCYTOMA; POINT MUTATION; RETINA TUMOR; VON HIPPEL LINDAU DISEASE;

ADRENAL GLAND NEOPLASMS; ADULT; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; FEMALE; HIPPEL-LINDAU DISEASE; HUMANS; LIGASES; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; PHEOCHROMOCYTOMA; TOMOGRAPHY, X-RAY COMPUTED; TUMOR SUPPRESSOR PROTEINS; UBIQUITIN-PROTEIN LIGASES; VON HIPPEL-LINDAU TUMOR SUPPRESSOR PROTEIN;

EID: 0034871115     PISSN: 09169636     EISSN: None     Source Type: Journal    
DOI: 10.1291/hypres.24.445     Document Type: Article

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