research A New Mutation in the Type II Hair Cortex Keratin hHb1 Involved in the Inherited Hair Disorder Monilethrix
A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.
Search
forLearn
0 / 0 results — no results
Research
5 / 98 resultsresearch An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.
research Hair Anomalies in a 6-Year-Old Girl
A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.
research A Mutation in the Type II Hair Keratin KRT86 Gene in a Han Family with Monilethrix
A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.
research Analysis of Human Hair Basic Keratin 6 Gene Mutation in a Chinese Han Family With Monilethrix
A gene mutation causes monilethrix in a Chinese family.
Community Join
0 / 0 results — no results