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Paper Details

SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy.
J Hum Genet
8
2019
Author NameAffiliation
Bj??rn Fischer-ZirnsakInstitut fur Medizinische Genetik und Humangenetik, Charite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt Universitat zu Berlin, and Berlin Institute of Health
Bj??rn Fischer-ZirnsakMax-Planck-Institut fuer Molekulare Genetik
Bj??rn Fischer-ZirnsakBerlin-Brandenburg Center for Regenerative Therapies (BCRT), Charite - Universitatsmedizin Berlin
Beyhan T??ys??zIstanbul University-Cerrahpasa
Stefan MundlosInstitut fur Medizinische Genetik und Humangenetik, Charite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt Universitat zu Berlin, and Berlin Institute of Health
Stefan MundlosMax-Planck-Institut fuer Molekulare Genetik
Stefan MundlosBerlin-Brandenburg Center for Regenerative Therapies (BCRT), Charite - Universitatsmedizin Berlin
Denise HornInstitut fur Medizinische Genetik und Humangenetik, Charite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt Universitat zu Berlin, and Berlin Institute of Health
Uwe KornakInstitut fur Medizinische Genetik und Humangenetik, Charite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt Universitat zu Berlin, and Berlin Institute of Health
Uwe KornakMax-Planck-Institut fuer Molekulare Genetik
Uwe KornakBerlin-Brandenburg Center for Regenerative Therapies (BCRT), Charite - Universitatsmedizin Berlin
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