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JOURNAL.PONE.0112747
JOURNAL.PONE.0112747
http://dx.doi.org/10.1371/JOURNAL.PONE.0112747
Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome.
P356
Q34506328-522E75A2-3C57-423A-AF4F-EC62AEF89695
P356
JOURNAL.PONE.0112747
http://dx.doi.org/10.1371/JOURNAL.PONE.0112747