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KALA SAMPAT, M.D.
M.D.
Pediatrics Physician
NPI: 1174583215Individual
Specialties, Licenses & Credentials
Research & Publications (4)
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
PMID 17960116·Mol Vis·2007
8-other
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.
PMID 17935237·Am J Med Genet A·2007
8-other
Protein kinase C negatively regulates Akt activity and modifies UVC-induced apoptosis in mouse keratinocytes.
PMID 16338928·J Biol Chem·2006
7-preclinical
No pathogenic mutations identified in the COL8A2 gene or four positional candidate genes in patients with posterior polymorphous corneal dystrophy.
PMID 15851557·Invest Ophthalmol Vis Sci·2005
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
- 503 W 1ST ST, SUITE B
BORGER, TX 79007 - Phone
- (806) 274-7111
Quick Facts
- NPI
- 1174583215
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 4
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