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Leah M Huber

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Clinical Genetics|February 1, 2025
Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a FamilyLeah M Huber, Aslı Subaşıoğlu, Dorota Garczarczyk-Asim, et al.
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Clinical Genetics|February 1, 2025
Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a FamilyLeah M Huber, Aslı Subaşıoğlu, Dorota Garczarczyk-Asim, et al.
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