S-EPMC5685937 - A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family. - OmicsDI

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A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family.

ABSTRACT:

SUBMITTER: Khan S

PROVIDER: S-EPMC5685937 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature