HIGHLIGHTS
- who: LSS mutation and colleagues from the University of Amsterdam, Netherlands Medicine, China have published the article: A novel homozygous mutation in LSS gene possibly causes hypotrichosis simplex in two siblings of a Tibetan family from the western Sichuan province of China, in the Journal: (JOURNAL)
- what: The work provided new insights into the etiology and pathogenesis of this genetic disease.
- how: This study was conducted in compliance with the principles of the Declaration of Helsinki.
SUMMARY
Hypotrichosis simplex (MIM 146520) is a rare form of monogenic alopecia. Patients . . .
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