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454526
454526
http://dx.doi.org/10.1155/2015/454526
Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1.
P356
Q36261015-1CF42283-4AEB-4B08-84AD-2BE058CDB49F
P356
454526
http://dx.doi.org/10.1155/2015/454526