Results
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14633.
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14634.
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A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents. [electronic resource] by
- Raas-Rothschild, Annick
- Wanders, Ronald J A
- Mooijer, Petra A W
- Gootjes, Jeannette
- Waterham, Hans R
- Gutman, Alisa
- Suzuki, Yasuyuki
- Shimozawa, Nobuyuki
- Kondo, Naomi
- Eshel, Gideon
- Espeel, Marc
- Roels, Frank
- Korman, Stanley H
Producer: 20020418
In:
American journal of human genetics vol. 70
Availability: No items available.
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