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- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Woolly hair generalizado: caso clínico e revisão da literatura
- Inherited Disorders of the Hair
- [Wooly hair syndrome. Clinical and microscopic study].
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Hair dysplasias
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Woolly Hair in Two Siblings
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Two females with hair loss
- Biology and Genetics of Hair
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Current Genetics in Hair Diseases
- Alopezien und Hypotrichosen im Kindesalter