[PDF][PDF] Carbonic anhydrase II deficiency: A novel mutation.
S Nampoothiri, Y Anikster - Indian pediatrics, 2009 - indianpediatrics.net
Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal recessive disorder,
characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A …
characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A …
Carbonic Anhydrase II Deficiency: A Novel Mutation.
S NAMPOOTHIRI, Y ANIKSTER - Indian Pediatrics, 2009 - search.ebscohost.com
Abstract Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal recessive
disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral …
disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral …
Carbonic anhydrase II deficiency a novel mutation.
S Nampoothiri, Y Anikster - Indian Pediatrics, 2009 - europepmc.org
Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal recessive disorder,
characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A …
characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A …
Carbonic anhydrase II deficiency: A novel mutation.
S Nampoothiri, Y Anikster - Indian Pediatr, 2009 - pesquisa.bvsalud.org
ABSTRACT Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal
recessive disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and …
recessive disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and …
Carbonic anhydrase II deficiency a novel mutation
S Nampoothiri, Y Anikster - Indian pediatrics, 2009 - pubmed.ncbi.nlm.nih.gov
Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal recessive disorder,
characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A …
characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A …
Carbonic anhydrase II deficiency: A novel mutation.
S Nampoothiri, Y Anikster - Indian Pediatr, 2009 - pesquisa.bvsalud.org
ABSTRACT Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal
recessive disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and …
recessive disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and …