Case Report: Novel homozygous MAN1B1mutation in two Italians patients with Rafiq syndrome.

Saved in:
Bibliographic Details
Title: Case Report: Novel homozygous MAN1B1mutation in two Italians patients with Rafiq syndrome.
Authors: Cotelli MS; Cognitive and Behavioural Neurology, ASST Spedali Civili, Spedali Civili 1 Square, Brescia, BS, 25100, Italy. mariasofia.cotelli1@unibs.it., Draghi A; Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Medical Genetic Unit, Milan, Italy., Bestetti I; Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Laboratory Genetic Unit, Milan, Italy., Bedeschi MF; Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Medical Genetic Unit, Milan, Italy., Borroni B; Cognitive and Behavioural Neurology, ASST Spedali Civili, Spedali Civili 1 Square, Brescia, BS, 25100, Italy.; Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2025 Apr; Vol. 46 (4), pp. 1937-1939. Date of Electronic Publication: 2024 Dec 09.
Publication Type: Letter
Journal Info: Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1590-3478 (Electronic) Linking ISSN: 15901874 NLM ISO Abbreviation: Neurol Sci Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
Full text is not displayed to guests.
Be the first to leave a comment!
You must be logged in first