Genotype/Phenotype Correlation of MORC2 Mutations
Conditions
Charcot Marie Tooth Disease · DIFGAN · Developmental Delay (Disorder) · Impaired Growth · Dysmorphic Facies and Axonal Neuropathy
Simple summaryAI-assisted
This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.
Locations
CHU de Besançon, Besançon, France
CHRU Brest, Brest, France
Contact: Study coordinator (Audebert Bellanger, MD)CHU Grenoble, Grenoble, France
CH de Versailles, Le Chesnay, France
Service de Génétique moléculaire, pharmacogénétique, hormologie Hôpital Bicêtre, Le Kremlin-Bicêtre, France
Hospices Civils de Lyon, Lyon, France
CHU Marseille, Marseille, France
Contact: Study coordinator (Nathalie BONELLO, MD)CHU de Nantes, Nantes, France
CH Pitié Salpêtrière, Paris, France
Hôpital Necker, Paris, France
CHU de Saint-Etienne, Saint-Etienne, France
Contact: Study coordinator (Jean-Philippe Camdessanche, MD) · j.philippe.camdessanche@chu-st-etienne.fr · 0033477127805CHU Strasbourg, Strasbourg, France
Contact: Study coordinator (Aleksandra NADAJ PAKLEZA)