Associated Papers
Talin variant P229S compromises integrin activation and associates with multifaceted clinical symptoms.
Azizi L et al.
Human Molecular Genetics, 2022
Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.
Deng H et al.
Plos One, 2016
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