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Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients
Zhou P,
Liu Y,
Lv F,
Nie M,
Jiang Y,
et al.
(2014)
Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients.
PLOS ONE 9(9): e107594.
https://doi.org/10.1371/journal.pone.0107594