Biallelic Variants in ARHGAP19 Cause a Progressive Inherited Motor-Predominant Neuropathy-An Update
Fecha de publicación:
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Dominik, N
- Efthymiou, S
- Record, C
- Miao, XY
- Lin, R
- Parmar, J
- Scardamaglia, A
- Maroofian, R
- Aughey, G
- Wilson, A
- Lowe, S
- Curro, R
- Schnekenberg, R
- Alavi, S
- Leclaire, L
- He, Y
- Zhelcheska, K
- Bellaiche, Y
- Gaugué, I
- Skorupinska, M
- Van de Vondel, L
- Da'as, S
- Turchetti, V
- Güngör, S
- Monahan, G
- Karimiani, EG
- Jamshidi, Y
- Lamont, P
- Ricaurte, CA
- Topaloglu, H
- Jordanova, A
- Zaman, M
- Banu, S
- Marques, W
- Tomaselli, PJ
- Aynekin, B
- Cansu, A
- Per, H
- Güleç, A
- Alvi, JR
- Sultan, T
- Khan, A
- Zifarelli, G
- Ibrahim, S
- Mancini, G
- Motazacker, MM
- Brusse, E
- Lupo, V
- Basak, AN
- Tekgul, S
- Palvadeau, R
- Baets, J
- Parman, Y
- Çakar, A
- Horvath, R
- Haack, T
- Stahl, JH
- Grundmann-Hauser, K
- Park, J
- Züchner, S
- Laing, N
- Wilson, L
- Rossor, A
- Polke, J
- Figueiredo, FB
- Pessoa, AL
- Kok, F
- Coimbra-Neto, AR
- França, M
- Ravenscroft, G
- Hamed, SA
- Chung, W
- Osborn, D
- Hanna, M
- Cortese, A
- Reilly, M
- Jepson, J
- Lamarche-Vane, N
- Houlden, H
Grupos
Abstract
Abstract no disponible
Filiaciones
Filiaciones no disponibles
Keywords
- ARHGAP19; CMT; Neuropathy; Charcot-Marie-Tooth; Rho-pathway
Cita
Dominik,N,Efthymiou,S,Record,C,Miao,XY,Lin,R,Parmar,J,Scardamaglia,A et al. Biallelic Variants in ARHGAP19 Cause a Progressive Inherited Motor-Predominant Neuropathy-An Update. 111 RIVER ST, HOBOKEN 07030-5774, NJ:WILEY. 2025 p.p. 24-25.
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