Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency

Test Type : Molecular
Test Name : Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency
Gene Name : CHRNE
OMIM No : 100725
Phenotype Number : 608931
LOKASYON GRCh38 : 17:4,897,770-4,905,018
Sample Type : EDTA BLOOD
Result Time : 45-60 Day
Type of Transfer : 4° / 30°
SUT Code : G100390
Transaction Name : Next Generation DNA Sequencing, 1 Gen
Method : Sequencing
Ref SEQ : NM_000080
Other informations :