Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata - Concepedia

Concepedia

Publication | Closed Access

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

445

Citations

57

References

1997

Year

Nancy Braverman, Gary Steel, Cassandra Obie, Ann B. Moser, Hugo W. Moser, Stephen J. Gould, David Valle‐García

Nature Genetics

Rhizomelic Chondrodysplasia PunctataSignal TransductionBone Morphogenic ProteinMedicineHuman Pex7PathologyPeroxisomal Pts2 ReceptorCell BiologyCell SignalingConnective Tissue Disease

References

	Year	Citations

Page 1