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  1. 1
    "Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D."
    Honsho M., Tamura S., Shimozawa N., Suzuki Y., Kondo N., Fujiki Y.
    Am. J. Hum. Genet. 63:1622-1630(1998) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), INVOLVEMENT IN PBD-CG9 AND PBD8A, VARIANT ILE-116.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  2. 13
    Cited for: VARIANTS PBD8B VAL-252 DEL; THR-289 AND CYS-331.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
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