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ABDUL MANNAN, DO
DO
Internal Medicine Physician
NPI: 1245971498Individual
Specialties, Licenses & Credentials
Research & Publications (20)
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein.
PMID 16602018·Neurogenetics·2006
7-preclinical
ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia.
PMID 16826525·Am J Hum Genet·2006
4-observational
Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse.
PMID 15503243·Neurogenetics·2004
7-preclinical
Calgizarrin like gene (Cal) deficient mice undergo normal spermatogenesis.
PMID 14579419·Mol Reprod Dev·2003
7-preclinical
Male mice lacking the Theg (testicular haploid expressed gene) protein undergo normal spermatogenesis and are fertile.
PMID 12748127·Biol Reprod·2003
4-observational
Alternative splicing, chromosome assignment and subcellular localization of the testicular haploid expressed gene (THEG).
PMID 11173852·Cytogenet Cell Genet·2000
7-preclinical
Vascular hamartoma of the paranasal sinuses: report of 3 rare cases and a short review of the literature.
PMID 19172571·Ear Nose Throat J·2009
6-review
Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia.
PMID 18701882·Eur J Hum Genet·2009
8-other
Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia.
PMID 18190593·Clin Genet·2008
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
- 127 NORTH ST
BATAVIA, NY 14020 - Phone
- (585) 344-7269
Locations (5)
Quick Facts
- NPI
- 1245971498
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 5
- Publications
- 20
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