Publishing research using ab92950? Please let us know so that we can cite the reference in this datasheet.
ab92950 has been referenced in 1 publication.
Logan CV et al.Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII a1 Chain.Am J Hum Genet 97:878-85 (2015).
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