41094-4LOINC 2.82
LAMA2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
LAMA2 gene Mut Anl Bld/T
Component
- LAMA2 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; Laminin M; laminin, alpha 2; Laminin, alpha 2 (merosin, congenital muscular dystrophy) gene; LAMM; Merosin heavy chain; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- LAMA2 gene targeted mutation analysis
- Laminin M
- laminin, alpha 2
- Laminin, alpha 2 (merosin, congenital muscular dystrophy) gene
- LAMM
- Merosin heavy chain
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue