| 1 | RHAG, RHNR
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| Rhmod syndrome : a family study of the translation-initiator mutation in the Rh50 glycoprotein gene.
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| Huang CH, et al.
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| Am J Hum Genet 64 : 108-117. 1999
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| 2 | RHAG, RHNR
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| A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type.
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| Hyland CA, Cherif-Zahar B, Cowley N, Raynal V, Parkes J, Saul A, Cartron JP.
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| Blood 91(4):1458-63. 1998
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| 3 | RHAG, RHNR
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| The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease.
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| Huang CH.
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| J Biol Chem 273(4):2207-13. 1998
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| 4 | RHAG, RHNR
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| A splicing mutation of the RHAG gene associated with the RHnull phenotype.
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| Kawano M, et al.
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| Ann Hum Genet 62 : 107-113. 1998
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| 5 | RHAG, RHCE, RHNR
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| Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment.
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| Huang CH, Liu Z, Cheng G, Chen Y.
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| Blood 92 : 1776-1784. 1998
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| 6 | RHAG, RHNR
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| Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene.
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| Cherif-Zahar B, et al.
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| Blood 92 : 2535-2540. 1998
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| 7 | RHAG, RHNR
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| Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency.
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| Cherif-Zahar B, et al.
|
| Nat Genet 12 : 168-173. 1996
|