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MUSSA MUSTAPHA, PHARM.D.
PHARM.D.
Pharmacist
NPI: 1124385679Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
5302038283(MI)
Research & Publications (19)
Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.
PMID 19176829·J Neurosci·2009
7-preclinical
Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.
PMID 17619105·J Assoc Res Otolaryngol·2007
4-observational
Taxonomy and inventory of the cytospecies and cytotypes of the Simulium damnosum complex (Diptera: Simuliidae) in relation to onchocerciasis.
PMID 18045261·Trop Med Int Health·2007
7-preclinical
Complexity and integration in the control of inner-ear development.
PMID 17915040·Genome Biol·2007
7-preclinical
Revision of the Ketaketa subcomplex of blackflies of the Simulium damnosum complex.
PMID 16608492·Med Vet Entomol·2006
4-observational
Incrimination of Simulium thyolense (Diptera: Simuliidae) as the anthropophilic blackfly in the Thyolo focus of human onchocerciasis in Malawi.
PMID 15814037·Ann Trop Med Parasitol·2005
7-preclinical
The cytotaxonomy and morphotaxonomy of Simulium mengense (Diptera: Simuliidae).
PMID 15257801·Ann Trop Med Parasitol·2004
7-preclinical
A new cytotype of Simulium squamosum from south-west Cameroon.
PMID 15347398·Med Vet Entomol·2004
7-preclinical
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
PMID 12833159·Nat Genet·2003
7-preclinical
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
PMID 12588794·Hum Mol Genet·2003
8-other
Cytotaxonomy, morphology and molecular systematics of the Bioko form of Simulium yahense (Diptera: Simuliidae).
PMID 12699536·Bull Entomol Res·2003
7-preclinical
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations.
PMID 12080392·Eur J Hum Genet·2002
8-other
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.
PMID 11972037·Proc Natl Acad Sci U S A·2002
7-preclinical
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
PMID 11941484·Hum Genet·2002
8-other
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
PMID 11973626·Eur J Hum Genet·2002
8-other
Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.
PMID 11584050·J Med Genet·2001
8-other
Exclusion of chromosome 15q21.1 in autosomal-recessive Weill-Marchesani syndrome in an inbred Lebanese family.
PMID 11149617·Clin Genet·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 7621 CHASE RD
DEARBORN, MI 48126 - Phone
- (313) 584-7621
Quick Facts
- NPI
- 1124385679
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 19
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