Molecular Modelling and Dynamics of CA2 Missense Mutations Causative to Carbonic Anhydrase 2 Deficiency Syndrome

Noor Ahmad Shaik,Hifaa A. Bokhari,Tariq Ahmed Masoodi,Preetha J. Shetty,Ghada Ajabnoor,Ramu Elango,Babajan Banaganapalli

Molecular Modelling and Dynamics of CA2 Missense Mutations Causative to Carbonic Anhydrase 2 Deficiency Syndrome

2019

Noor Ahmad Shaik
Hifaa A. Bokhari
Tariq Ahmed Masoodi
Preetha J. Shetty
Ghada Ajabnoor
Ramu Elango
Babajan Banaganapalli

AbstractCarbonic anhydrase 2 (CA2) enzyme deficiency caused by CA2 gene mutations is an inherited disorder characterized by symptoms like osteopetrosis, renal tubular acidosis, and cerebral calcifi...

Keywords:

Carbonic anhydrase
Missense mutation
Biochemistry
Chemistry
gene mutation
Enzyme deficiency
deficiency syndrome
Molecular biology
Cerebral calcification
Renal tubular acidosis
Osteopetrosis

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