An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis

Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion

Ana Kljuic, Hisham Bazzi, John P. Sundberg et al. · Cell · 2003 · 325 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +16

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

Hermelita Winter, Mike A. Rogers, Lutz Langbein et al. · Nature Genetics · 1997 · 176 citations

Medicine, Dermatology, Genetics +14

A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix

Hermelita Winter, Michael A. Rogers, Mathias Gebhardt et al. · Human Genetics · 1997 · 100 citations

Medicine, Dermatology, Genetics +14

A missense mutation in the type II hair keratin hHb3 is associated with monilethrix

Maurice A. M. Van Steensel · Journal of Medical Genetics · 2005 · 79 citations · Full text

Medicine, Dermatology, Genetics +15

Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype

Bernhard Korge, Henning Hamm, Catherine S. Jury et al. · Journal of Investigative Dermatology · 1999 · 62 citations · Full text

Medicine, Dermatology, Genetics +17