January 15, 2009

Familial interstitial disease with I73T mutation: A mid‐ and long‐term study

RTRola Abou TaamHôpital Necker-Enfants Malades FJFrancis JaubertHôpital Necker-Enfants Malades SES. EmondHôpital Necker-Enfants Malades

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Abstract

This kindred illustrates the variability of respiratory involvement and prognosis. It confirms the value of genetic screening for surfactant protein genes mutations.

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Taam et al. (Thu,) studied this question.

synapsesocial.com/papers/69dd48297808b00a4799c163 https://doi.org/https://doi.org/10.1002/ppul.20970

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