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Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4
by
Tóth, Lola
,
Fábos, Beáta
,
Farkas, Katalin
,
Sulák, Adrienn
,
Tripolszki, Kornélia
,
Széll, Márta
,
Nagy, Nikoletta
Published in
BMC medical genetics
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Delineating the genetic heterogeneity of OCA in Hungarian patients
by
Fábos, Beáta
,
Farkas, Katalin
,
Tóth, Lola
,
Sulák, Adrienn
,
Tripolszki, Kornélia
,
Tihanyi, Mariann
,
Németh, Réka
,
Vas, Krisztina
,
Csoma, Zsanett
,
Kemény, Lajos
,
Széll, Márta
,
Nagy, Nikoletta
Published in
European journal of medical research
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CTSC and Papillon–Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update
by
Nagy, Nikoletta
,
Vályi, Péter
,
Csoma, Zsanett
,
Sulák, Adrienn
,
Tripolszki, Kornélia
,
Farkas, Katalin
,
Paschali, Ekaterine
,
Papp, Ferenc
,
Tóth, Lola
,
Fábos, Beáta
,
Kemény, Lajos
,
Nagy, Katalin
,
Széll, Márta
Published in
Molecular genetics & genomic medicine
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CTSC and Papillon–Lefèvre syndrome: detection of recurrent mutations in H ungarian patients, a review of published variants and database update
by
Nagy, Nikoletta
,
Vályi, Péter
,
Csoma, Zsanett
,
Sulák, Adrienn
,
Tripolszki, Kornélia
,
Farkas, Katalin
,
Paschali, Ekaterine
,
Papp, Ferenc
,
Tóth, Lola
,
Fábos, Beáta
,
Kemény, Lajos
,
Nagy, Katalin
,
Széll, Márta
Published in
Molecular genetics & genomic medicine
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