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Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency
by
Ziemnicka, K.
,
Budny, B.
,
Drobnik, K.
,
Baszko-Błaszyk, D.
,
Stajgis, M.
,
Katulska, K.
,
Waśko, R.
,
Wrotkowska, E.
,
Słomski, R.
,
Ruchała, M.
Published in
Journal of applied genetics
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Journal Of Applied Genetics
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Adult
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Amino Acid Sequence
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Animal Genetics And Genomics
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Biomedical And Life Sciences
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Biotechnology & Applied Microbiology
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Combined Pituitary Hormone Deficiency
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Cphd
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Developmental Biology
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Dna Binding Proteins
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Frameshift Mutation
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Genetic Aspects
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Genetic Transcription
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Genetics & Heredity
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Heterozygote
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Homeodomain Proteins - Genetics
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Human Genetics
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Human Genetics • Case Report
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Humans
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Hypopituitarism - Genetics
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Life Sciences
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