Associated Papers
A novel deletion mutation in the ATP6V0A2 gene in an Iranian patient affected by autosomal recessive cutis laxa.
Shafagh Shishavan N et al.
Irish Journal of Medical Science, 2023
Review of clinical and molecular variability in autosomal recessive cutis laxa 2A.
Morlino S et al.
American Journal of Medical Genetics. Part A, 2021
A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing
Karacan İ et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology, 2019
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