Hypocalcemia, autosomal dominant, with Bartter syndrome

Test Type : Molecular
Test Name : Hypocalcemia, autosomal dominant, with Bartter syndrome
Gene Name : CASR
OMIM No : 601199
Phenotype Number : 601198
LOKASYON GRCh38 : 3:122,183,667-122,291,628
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_000388
Other informations :