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Siblings with biallelic TGFBR1 mutations and profound connective tissue disease: recessive Loeys-Dietz syndrome
Siblings with biallelic TGFBR1 mutations and profound connective tissue disease: recessive Loeys-Dietz syndrome
2021
Lois J. Starr
Mark E. Lindsay
Anji T. Yetman
Keywords:
Connective tissue disease
Pathology
Medicine
Loeys–Dietz syndrome
Correction
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