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AJMG.A.35983
AJMG.A.35983
http://dx.doi.org/10.1002/AJMG.A.35983
Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies
P356
Q57147671-BE666425-0F9C-47E2-B20C-C397552B5A25
P356
AJMG.A.35983
http://dx.doi.org/10.1002/AJMG.A.35983