Publication
| Honsho M, Tamura S, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y, Mutation in PEX16 is causal in the peroxisome-deficient zellweger syndrome of complementation group D [In Process Citation] Am J Hum Genet63:1622-30 1998 |
| PubMed ID: 9837814 |
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| Records Return:
(1)
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| Catalog ID | Gender | Age at Sampling | Description | Collection_Type_id |
| GM06231 | Female | 1 MO | PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A | GM |
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