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Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
Sharma P,
Reichert M,
Lu Y,
Markello TC,
Adams DR,
et al.
(2019)
Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype.
PLOS Genetics 15(5): e1008143.
https://doi.org/10.1371/journal.pgen.1008143