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Article

Filamin A gene mutation in an infant with progressive pulmonary emphysema, periventricular nodular heterotopia and congenital heart disease.

BMJ case reports - 4 Jan 2024

Khera Sanjeev, Jauhari Shilpa, Pattanayak Somali, Choubey Mrigank

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Identifiers

PMID: 38176754
DOI: 10.1136/bcr-2023-257676
PMCID: PMC10773292

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Filamin A gene mutation in an infant with progressive pulmonary emphysema, periventricular nodular heterotopia and congenital heart disease.PMID 38176754Read ↗

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