ArticleClinical genetics2024
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome.
Rabia Faridi et al.PubMed ↗Full text ↗Publisher ↗
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ArticleClinical genetics2024
Rabia Faridi et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.