MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations. (2013)

First Author: De Rocco D

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ejmg.2012.10.009

PubMed Identifier: 23123319

Publication URI: http://europepmc.org/abstract/MED/23123319

Type: Journal Article/Review

Volume: 56

Parent Publication: European journal of medical genetics

Issue: 1

ISSN: 1769-7212