Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS).

Abstract	A TaqI RFLP was detected within the ClCN4 gene, which lies between the loci for OA1 and MLS. There were no observed recombinations between this RFLP and the OA1 mutation in three informative families. Thus, the marker will be useful for genetic counseling in OA1.
Authors	R E Schnur, P A Wick
Journal	Human genetics (Hum Genet) Vol. 95 Issue 5 Pg. 594-5 (May 1995) ISSN: 0340-6717 [Print] Germany
PMID	7759088 (Publication Type: Journal Article)
Chemical References	Genetic Markers DNA Taq Polymerase DNA-Directed DNA Polymerase
Topics	Albinism, Ocular (genetics) Alleles Chromosome Mapping DNA (analysis) DNA-Directed DNA Polymerase Female Gene Frequency Genetic Linkage (genetics) Genetic Markers Humans Male Microphthalmos (genetics) Pedigree Polymorphism, Restriction Fragment Length Skin Diseases (genetics) Syndrome Taq Polymerase X Chromosome

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!