par Corben, Louise A.;Collins, Veronica;Milne, Sarah;Farmer, Jennifer;Musheno, Ann;Lynch, David;Subramony, Sub;Pandolfo, Massimo;Schulz, Jörg B.;Lin, Kim;Delatycki, Martin B;Akhlaghi, Hamed;Bidichandani, Sanjay I.;Boesch, Sylvia;Cnop, Miriam ;Corti, Manuela;Duquette, Antoine;Durr, Alexandra;Eigentler, Andreas;Emmanuel, Anton;Flynn, John M.;Foroush, Noushin Chini;Fournier, Anne;França, Marcondes C.;Giunti, Paola;Goh, Ellen;Graf, Lisa;Hadjivassiliou, Marios;Huckabee, Maggie-Lee;Kearney, Mary G.;Koeppen, Arnulf H.;Lie, Yenni;Lin, Kimberly Y.;Lowit, Anja;Mariotti, Caterina;Mathews, Katherine K.D.;McCormack, Shana E.;Montenegro, Lisa;Morlet, Thierry;Naeije, Gilles ;Panicker, Jalesh N.;Parkinson, Michael H.;Patel, Aarti;Payne, Ronald Mark;Perlman, Susan L;Peverill, Roger E.;Pousset, Francoise;Puccio, Hélène;Rai, Myriam ;Rance, Gary;Reetz, Kathrin;Rowland, Tennille;Sansom, Phoebe;Savvatis, Konstantinos;Schalling, Ellika;Schöls, Lüdger;Smith, Barbara;Soragni, Elisabetta;Spencer, Caroline;Synofzik, Matthis;Szmulewicz, David;Tai, Geneieve;Tamaroff, Jaclyn;Treat, Lauren;Carpentier, Ariane Veilleux;Vogel, Adam P.;Walther, Susan E.;Weber, David R.;Weisbrod, Neal;Wilmot, George;Wilson, Robert B.;Yoon, Grace;Zesiewicz, Theresa T.A.
Référence Orphanet journal of rare diseases, 17, 1
Publication Publié, 2022-12
Référence Orphanet journal of rare diseases, 17, 1
Publication Publié, 2022-12
Article révisé par les pairs
Titre: |
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Auteur: | Corben, Louise A.; Collins, Veronica; Milne, Sarah; Farmer, Jennifer; Musheno, Ann; Lynch, David; Subramony, Sub; Pandolfo, Massimo; Schulz, Jörg B.; Lin, Kim; Delatycki, Martin B; Akhlaghi, Hamed; Bidichandani, Sanjay I.; Boesch, Sylvia; Cnop, Miriam; Corti, Manuela; Duquette, Antoine; Durr, Alexandra; Eigentler, Andreas; Emmanuel, Anton; Flynn, John M.; Foroush, Noushin Chini; Fournier, Anne; França, Marcondes C.; Giunti, Paola; Goh, Ellen; Graf, Lisa; Hadjivassiliou, Marios; Huckabee, Maggie-Lee; Kearney, Mary G.; Koeppen, Arnulf H.; Lie, Yenni; Lin, Kimberly Y.; Lowit, Anja; Mariotti, Caterina; Mathews, Katherine K.D.; McCormack, Shana E.; Montenegro, Lisa; Morlet, Thierry; Naeije, Gilles; Panicker, Jalesh N.; Parkinson, Michael H.; Patel, Aarti; Payne, Ronald Mark; Perlman, Susan L; Peverill, Roger E.; Pousset, Francoise; Puccio, Hélène; Rai, Myriam; Rance, Gary; Reetz, Kathrin; Rowland, Tennille; Sansom, Phoebe; Savvatis, Konstantinos; Schalling, Ellika; Schöls, Lüdger; Smith, Barbara; Soragni, Elisabetta; Spencer, Caroline; Synofzik, Matthis; Szmulewicz, David; Tai, Geneieve; Tamaroff, Jaclyn; Treat, Lauren; Carpentier, Ariane Veilleux; Vogel, Adam P.; Walther, Susan E.; Weber, David R.; Weisbrod, Neal; Wilmot, George; Wilson, Robert B.; Yoon, Grace; Zesiewicz, Theresa T.A. |
Informations sur la publication: | Orphanet journal of rare diseases, 17, 1 |
Statut de publication: | Publié, 2022-12 |
Sujet CREF: | Médecine pathologie humaine |
Langue: | Anglais |
Identificateurs: | urn:issn:1750-1172 |
info:doi/10.1186/s13023-022-02568-3 | |
info:pii/2568 |