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NKX2 .1 run‐on mutation associated to familial brain–lung–thyroid syndrome
Author(s) -
Cavaliere Elena,
Gortan Anna Jolanda,
Passon Nadia,
Fabbro Dora,
Marin Dario,
Carecchio Miryam,
Baldan Federica,
Credendino Sara Carmela,
Gallo Rosa,
Cogo Paola,
Damante Giuseppe,
De Vita Gabriella
Publication year - 2021
Publication title -
clinical genetics
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.13961
Subject(s) - pediatrics , medicine , choreiform movement , psychology , endocrinology , dyskinesia , disease , parkinson's disease