LastName | mezghani |
FirstName | najla |
MiddleName | |
najla_mezghani2@yahoo.fr | |
OrganizationName | |
OrganizationURL | |
Country | Tunisia |
Address | |
PILastName | fakhfakh |
PIFirstName | faiza |
PIMiddleName | |
PIEmail | faiza.fakhfakh@gnet.tn |
OtherContributor | |
PolymorphismPosition | 6527 |
Polymorphism | T |
AlleleType | polymorphism |
NAChange | A-T |
AAChange | M-I |
Locus | MT-CO1 |
InsertPrePosition | |
InsertPostPosition | |
Insert | |
DeletionPosition | |
DeletionLength | |
OtherAllele | |
ComplexCategory | |
Detection | automated |
SampleID | mit33 |
Tissue | blood |
Phenotype | 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 |