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s12881-017-0414-7
s12881-017-0414-7
https://scigraph.springernature.com/pub.10.1186/s12881-017-0414-7
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome).
P2888
Q33651127-E2CB73EE-AA8E-4E67-816A-EBA06CDE83BA
P2888
s12881-017-0414-7
https://scigraph.springernature.com/pub.10.1186/s12881-017-0414-7