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2
AHG.12141
AHG.12141
http://dx.doi.org/10.1111/AHG.12141
Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma.
P356
Q50317484-D63353B6-97FD-4319-B567-1AAEEFDDCD75
P356
AHG.12141
http://dx.doi.org/10.1111/AHG.12141