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Chimeric CYP21A1P / CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia
by
Vrzalová, Zuzana
,
Hrubá, Zuzana
,
Hrabincová, Eva Sťahlová
,
Vrábelová, Slávka
,
Votava, Felix
,
Koloušková, Stanislava
,
Fajkusová, Lenka
Published in
European journal of medical genetics
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Mutation analysis of the ATP7B gene and genotype/phenotype correlation in 227 patients with Wilson disease
by
Vrabelova, Slavka
,
Letocha, Ondrej
,
Borsky, Marek
,
Kozak, Libor
Published in
Molecular genetics and metabolism
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European Journal Of Medical Genetics
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Molecular Genetics And Metabolism
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Genetics & Heredity
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Humans
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Life Sciences & Biomedicine
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Science & Technology
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21-Hydroxylase Deficiency
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Adenosine Triphosphatases - Genetics
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Adrenal Hyperplasia, Congenital - Genetics
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Allele Frequency
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Atp7B
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Base Sequence
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Cation Transport Proteins - Genetics
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Chimeric Gene
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Congenital Adrenal Hyperplasia
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Copper-Transporting Atpases
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Czechoslovakia
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Dna Mutational Analysis
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Dna Primers
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Electrophoresis, Polyacrylamide Gel
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Endocrinology & Metabolism
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Genotype
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Elsevier Sciencedirect Journals
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