(Q30989619)
English
autosomal dominant hypocalcemia 2
autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13
- HYPOC2
- HYPOCALCEMIA, AUTOSOMAL DOMINANT 2
- HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2
- Hypocalcemia, Autosomal Dominant type 2
- autosomal dominant hypocalcemia type 2
Statements
1 reference
2 references
Identifiers
1 reference
1 reference
1 reference
1 reference