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Volumn 36, Issue 3, 2009, Pages 419-424

RET mutation Tyr791Phe: The genetic cause of different diseases derived from neural crest

(9) Vaclavikova, Eliska a Dvorakova, Sarka a Sykorova, Vlasta a Bilek, Radovan a Dvorakova, Katerina a Vlcek, Petr b Skaba, Richard b Zelinka, Tomas c Bendlova, Bela a

a INSTITUTE OF ENDOCRINOLOGY (Czech Republic)

b UNIVERSITY HOSPITAL MOTOL (Czech Republic)

c CHARLES UNIVERSITY (Czech Republic)

Author keywords

Genetics; Hirschsprung's disease; Medullary thyroid carcinoma; Pheochromocytoma; RET mutation; RET proto oncogene

Indexed keywords

CYSTEINE; LEUCINE; METHIONINE; PHENYLALANINE; SERINE; THREONINE; TYROSINE;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; DNA POLYMORPHISM; EXON; FAMILY; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GENOTYPE; GERMLINE MICRONUCLEUS; HETEROZYGOTE; HIRSCHSPRUNG DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; NEURAL CREST; NEUROFIBROMATOSIS; PHENOTYPE; PHEOCHROMOCYTOMA; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTO ONCOGENE; SCHOOL CHILD; SIPPLE SYNDROME; THYROID MEDULLARY CARCINOMA;

ADOLESCENT; ADULT; AGED; AMINO ACID SUBSTITUTION; CARCINOMA, MEDULLARY; CHILD; DISEASE; FAMILY; FEMALE; GENETIC ASSOCIATION STUDIES; GERM-LINE MUTATION; HIRSCHSPRUNG DISEASE; HUMANS; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; NEURAL CREST; PHENYLALANINE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTO-ONCOGENE PROTEINS C-RET; THYROID NEOPLASMS; TYROSINE; YOUNG ADULT;

EID: 70449522035 PISSN: 1355008X EISSN: 15590100 Source Type: Journal
DOI: 10.1007/s12020-009-9242-7 Document Type: Article

Times cited : (21)

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