Pages that link to "Q47840650"

The following pages link to A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1 (Q47840650):

Displaying 17 items.

• Characterization of a 190-kilobase pair domain of human type I hair keratin genes (Q22003883) (← links)
• Keratins of the human hair follicle (Q28242328) (← links)
• Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene (Q33880598) (← links)
• Monilethrix: A New Family with the Novel Mutation in KRT81 Gene (Q34281420) (← links)
• Human hair keratin-associated proteins (KAPs). (Q36580843) (← links)
• A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix (Q36681883) (← links)
• Hair follicle-specific keratins and their diseases (Q36788686) (← links)
• Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues. (Q36809911) (← links)
• To grow or not to grow: hair morphogenesis and human genetic hair disorders (Q37705212) (← links)
• Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix (Q44373486) (← links)
• De novo mutations in monilethrix (Q44721678) (← links)
• Polymorphisms in the human high sulfur hair keratin-associated protein 1, KAP1, gene family (Q48283421) (← links)
• A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance (Q50495321) (← links)
• Novel KRT83 and KRT86 mutations associated with monilethrix. (Q50609840) (← links)
• A locus for hereditary hypotrichosis localized to human chromosome 18q21.1. (Q64968639) (← links)
• [Genetically induced hair diseases] (Q73866479) (← links)
• [Alopecia and hypotrichosis in childhood: clinical features and diagnosis] (Q88018485) (← links)