Egyptian Journal of Medical Human Genetics [The]. 2017; 18 (2): 193-197
in English
| IMEMR
| ID: emr-188482
ABSTRACT
Background:
Multiple endocrine neoplasia type 2A [MEN2A] is a rare cancer associated-syndrome, inherited in an autosomal dominant fashion and caused by germline mutation in RET proto-oncogene
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Pheochromocytoma
/
Arab World
/
Proto-Oncogene Proteins c-ret
/
Genetic Counseling
/
Mutation
Type of study:
Case report
Limits:
Adolescent
/
Adult
/
Aged
/
Female
/
Humans
/
Male
Language:
English
Journal:
Egypt. J. Med. Hum. Genet.
Year:
2017
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