Loss of heterozygosity at microsatellite marker localised near the metalloproteinase gene in patients with PEX syndrome;Utrata heterozygotyczności w markerze mikrosatelitarnym zlokalizowanym w pobliżu genu metaloproteinazy u chorych z zespołem pseudoeksfoliacji

Klinika Oczna

Volumn 106, Issue 1-2 SUPPL., 2004, Pages 153-154

  Zalewska, Renata ^a,c   Mariak, Zofia ^a   Pepiński, Witold ^b   Wojnar, Małgorzata ^a   Proniewska Skrȩtek, Ewa ^a   Skawrońska, Małgorzata ^b   Janica, Jerzy ^b  

^a Z Kliniki Okulistyki Akademii Medycznej W Bia ymstoku

^b Z Zak adu Medycyny Sa dowej Akademii Medycznej W Bia ymstoku

^c Klinika Okulistyki AMB   (Poland)

Author keywords

Loss of heterozygosity (LOH); Metalloproteinases; Pseudoexfoliation syndrome

Indexed keywords

METALLOPROTEINASE; MICROSATELLITE DNA;

AGED; ARTICLE; EXFOLIATION SYNDROME; FEMALE; GENETICS; HETEROZYGOSITY LOSS; HUMAN; IRIS; LENS CAPSULE; LENS NUCLEUS; MALE; METABOLISM; METHODOLOGY; MIDDLE AGED; POLYMERASE CHAIN REACTION;

AGED; AGED, 80 AND OVER; EXFOLIATION SYNDROME; FEMALE; HUMANS; IRIS; LENS CAPSULE, CRYSTALLINE; LENS NUCLEUS, CRYSTALLINE; LOSS OF HETEROZYGOSITY; MALE; METALLOPROTEASES; MICROSATELLITE REPEATS; MIDDLE AGED; POLYMERASE CHAIN REACTION;

EID: 16644401637     PISSN: 00232157     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (9)

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