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HIBA RISHEG, PH.D.
PH.D.
NPI: 1881799823Individual
Specialties, Licenses & Credentials
Ph.D. Medical GeneticsPrimary
Medical Genetics, Ph.D. Medical Genetics
Code: 170100000X
2005138
Research & Publications (5)
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene.
PMID 17369503·J Med Genet·2007
4-observational
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.
PMID 17334363·Nat Genet·2007
8-other
Biochemical abnormality in erythropoietic protoporphyria: cause and consequences.
PMID 16819399·J Pediatr Gastroenterol Nutr·2006
8-other
Molecular studies of liver disease in erythropoietic protoporphyria.
PMID 15758654·J Clin Gastroenterol·2005
6-review
Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver disease.
PMID 11929052·Cell Mol Biol (Noisy-le-grand)·2002
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 201 SAGE RD STE 300
CHAPEL HILL, NC 27514 - Phone
- (919) 942-0021
Quick Facts
- NPI
- 1881799823
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 5
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