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Unpublished Variant 20100125002

This is a record of an observed human mtDNA variant submitted to MITOMAP

Submitters may return to this page at any time to update the information. Submitters who wish to amend a record submitted before November 2009 must register and send an email to mitomap@email.chop.edu to obtain editing privileges on the page.
Submitted by: NajlaMezghani
MITOMAP list of submitted variants
MITOMASTER allele analysis

Citing this variant:
mezghani, najla; fakhfakh, faiza 2010. MITOMAP mtDNA Sequence Data, https://www.mitomap.org/foswiki/bin/view/MITOMAP/Submissions/20100125002

VariantSubmissionForm edit

LastName	mezghani
FirstName	najla
MiddleName
Email	najla_mezghani2@yahoo.fr
OrganizationName
OrganizationURL
Country	Tunisia
Address
PILastName	fakhfakh
PIFirstName	faiza
PIMiddleName
PIEmail	faiza.fakhfakh@gnet.tn
OtherContributor
PolymorphismPosition	16230
Polymorphism	T
AlleleType	polymorphism
NAChange	A-T
AAChange	non-coding
Locus	Control Region
InsertPrePosition
InsertPostPosition
Insert
DeletionPosition
DeletionLength
OtherAllele
ComplexCategory
Detection	automated
SampleID	mit33
Tissue	blood
Phenotype	diabetes;bilateral sensorineural hearing loss, mental and language disorder, bilateral cataract, retinitis pigmentosa, pyramidal syndrome with calcification of basal ganglia and epilepsy
Ethnicity	Tunisian
Origin	Tunisia
Haplogroup
Comment

Topic revision: r1 - 29 Mar 2013, UnknownUser

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