Work

Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: Implication for the MRX locus

Year: 1996

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics

DOI: 10.1002/(sici)1096-8628(19960906)64:4<583::aid-ajmg11>3.0.co;2-d

Authors: Koji Muroya, Tsutomu Ogata, Nobutake Matsuo, Toshiro Nagai, Brunella Franco, Andrea Ballabio, Gudrun Rappold, Nobiro Sakura, Yoshimitsu Fukushima

Institutions: Keio University, Tokyo Metropolitan Kiyose Children's Hospital, Telethon Institute Of Genetics And Medicine, Heidelberg University, Hiroshima University, Shinshu University

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Fondation pour la Recherche Médicale

OpenAlex ID: W2025512845

FWCI: 1.002

Cites: 31

Cited by: 26

Related to: 10