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- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Discreet monilethrix: De novo mutation on the example of polish families
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- <i>De novo</i> mutations in monilethrix
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
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