Evaluation of a genetic test for diagnose of primary hypolactasia in Khorasan

Iranian Journal of Basic Medical Sciences

Volumn 15, Issue 6, 2012, Pages 1127-1130

  Alizadeh, Maryam ^a   Sadr Nabavi, Ariane ^a,b  

^a MASHHAD UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b AVICENNA RESEARCH INSTITUTE   (Iran)

Author keywords

Hypolactasia; Iranian population; LPH

Indexed keywords

GENOMIC DNA; LACTASE;

ADULT; ARTICLE; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DNA EXTRACTION; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPING TECHNIQUE; HUMAN; LACTASE DEFICIENCY; MAJOR CLINICAL STUDY; MALE; PERIPHERAL BLOOD MONONUCLEAR CELL; POLYMERASE CHAIN REACTION; PRIMARY HYPOLACTASIA; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84869024433     PISSN: 20083866     EISSN: 20083874     Source Type: Journal    
DOI: None     Document Type: Article

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