Unknown

Dataset Information

0

Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by LIPH Pathogenic Variants.

ABSTRACT:

SUBMITTER: Taki T 

PROVIDER: S-EPMC7364366 | biostudies-literature | 2020 Oct

REPOSITORIES: biostudies-literature

Json Xml
altmetric image

Publications

Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by LIPH Pathogenic Variants.

Taki Tomoki T   Tanahashi Kana K   Takeichi Takuya T   Yoshikawa Takenori T   Murase Yuya Y   Sugiura Kazumitsu K   Akiyama Masashi M  

JAMA dermatology 20201001 10

Similar Datasets

Unknown Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations.
| S-EPMC3929696 | biostudies-literature
Unknown Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family.
| S-EPMC4211517 | biostudies-literature
Unknown Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis.
| S-EPMC2859194 | biostudies-literature
Unknown A case of autosomal recessive woolly hair/hypotrichosis with alternation in severity: deterioration and improvement with age.
| S-EPMC3901624 | biostudies-literature
Unknown Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis.
| S-EPMC3979697 | biostudies-literature
Unknown Unusual Clinical Presentation of Autosomal Recessive Woolly Hair.
| S-EPMC7109382 | biostudies-literature
Unknown A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair.
| S-EPMC5090258 | biostudies-literature
Unknown Complete defect in PA-PLA<sub>1</sub>α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous <i>LIPH</i> variant study in a Chinese pedigree.
| S-EPMC12098026 | biostudies-literature
Unknown Autosomal recessive ichthyosis with hypotrichosis caused by a mutation in ST14, encoding type II transmembrane serine protease matriptase.
| S-EPMC1821100 | biostudies-literature
Unknown Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis.
| S-EPMC7405639 | biostudies-literature