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searching for Monilethrix 2 found (18 total)

KRT81 (817 words) [view diff] exact match in snippet view article find links to article

KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix. GRCh38: Ensembl release 89: ENSG00000205426 – Ensembl, May 2017 GRCm38:

Lidia Rudnicka (2,946 words) [view diff] exact match in snippet view article find links to article

evaluation in genetic hair shaft abnormalities such as Netherton syndrome, monilethrix, wooly hair syndrome, pili torti, pili annulati and trichothiodystrophy