[…] areata Alopecia universalis Alopecia totalis Aganglionic megacolon Abnormal spermatogenesis Multifactorial inheritance Progressive alopecia Abnormal T-wave Curly hair Hypoplasia
[mendelian.co]
12] Wilson, N.J., Perez, M.L.C., Vahlquist, A., Schwartz, M.E., Hansens, C.D., McLean, W.H.I., et al. (2012) Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia
[scirp.org]
Authors, Source MeSH Adult Alopecia Blister Bone Diseases Cataract Child, Preschool Cornea Darier Disease Eye Diseases Female Humans Intellectual Disability Keratosis Leukoplakia
[unboundmedicine.com]