Reactome | Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis

author	[Person:9841195] Magini, P [Person:9841231] Smits, DJ [Person:9841236] Vandervore, L [Person:5229158] Schot, R [Person:9841228] Columbaro, M [Person:9841215] Kasteleijn, E [Person:9841223] van der Ent, M [Person:9841213] Palombo, F [Person:5229120] Lequin, MH [Person:9841200] Dremmen, M [Person:9841222] de Wit, MCY [Person:9841216] Severino, M [Person:9841224] Divizia, MT [Person:9841205] Striano, P [Person:9841218] Ordonez-Herrera, N [Person:9841203] Alhashem, A [Person:9841210] Al Fares, A [Person:9841217] Al Ghamdi, M [Person:8877960] Rolfs, A [Person:5320313] Bauer, P [Person:3662316] Demmers, J [Person:5229096] Verheijen, FW [Person:9841198] Wilke, M [Person:9841237] van Slegtenhorst, M [Person:5229117] van der Spek, PJ [Person:9841221] Seri, M [Person:9841206] Jansen, AC [Person:5610290] Stottmann, RW [Person:9841239] Hufnagel, RB [Person:9841197] Hopkin, RJ [Person:9841233] Aljeaid, D [Person:9698144] Wiszniewski, W [Person:9841238] Gawlinski, P [Person:9841241] Laure-Kamionowska, M [Person:4839835] Alkuraya, FS [Person:9841193] Akleh, H [Person:9841194] Stanley, V [Person:9841199] Musaev, D [Person:3621805] Gleeson, JG [Person:5602220] Zaki, MS [Person:195672] Brunetti-Pierri, N [Person:9841234] Cappuccio, G [Person:9841211] Davidov, B [Person:9841196] Basel-Salmon, L [Person:9841204] Bazak, L [Person:9841227] Shahar, NR [Person:9841219] Bertoli-Avella, A [Person:9841201] Mirzaa, GM [Person:4420023] Dobyns, WB [Person:9841235] Pippucci, T [Person:5649765] Fornerod, M [Person:9817395] Mancini, GMS
created	[InstanceEdit:9841226] Stephan, Ralf, 2023-08-11
dbId	9841229
displayName	Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
journal	Am J Hum Genet
pages	689-705
pubMedIdentifier	31495489
schemaClass	LiteratureReference
title	Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
url	http://www.ncbi.nlm.nih.gov/pubmed/31495489
volume	105
year	2019

Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis Show undefined attributes

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