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frameshift mutations
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Curated Studies
Most Correlated Studies
Li-Fraumeni syndrome causative mutations and the effect on breast epithelial and stromal cells
Retinas from CRX mutant mice with Leber congenital amaurosis phenotype
Caudal epididymis, oviduct, uterus, and vas deferens with Hoxa9/10/11 and Hoxd9/10/11 knockout
Lymphoblastoid cell cultures from Cornelia de Lange, Alagille, and Roberts syndrome patients
T-cell acute lymphoblastic leukemia Jurkat cells with heterozygous BRCA2 mutant clones
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Literature
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A homozygous frameshift mutation in the HOXC13 gene underlies pure hair and nail ectodermal dysplasi…
Prophylactic administration of prothrombin complex concentrates for congenital prothrombin deficienc…
Identification of a novel frameshift mutation of human androgen receptor gene in a patient featuring…
A new β⁰-thalassemia frameshift mutation [β 48 (-T)] in a Uruguayan family.
Two novel frameshift mutations of the DSRAD gene in Chinese pedigrees with dyschromatosis symmetrica…
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Frameshift Peptides of Children With NF1
Biochemical Response to Interferon-Gamma in Subjects With Specific Gene Mutation in Chronic Granulom…
Phase II Study of Tazemetostat in Solid Tumors Harboring an ARID1A Mutation
Gene Mutations and Orthopaedic Symptoms Correlation of Multiple Hereditary Exostoses: Multicentre Pr…
Tremelimumab, Durvalumab, and Belinostat for the Treatment of ARID1A Mutated Metastatic or Unresecta…
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