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517616
517616
http://dx.doi.org/10.1086/517616
Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype.
P356
Q35752656-1752140F-C9A7-4C1A-94DB-6DF9909C481C
P356
517616
http://dx.doi.org/10.1086/517616