4.4 Article

Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype

Khalid Al-Thihli et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)

Article Clinical Neurology

Phenotypic clustering in MPZ mutations

ME Shy et al.

BRAIN (2004)

Article Neurosciences

Peripheral myelin protein 22 kDa and protein zero:: domain specific trans-interactions

B Hasse et al.

MOLECULAR AND CELLULAR NEUROSCIENCE (2004)

Article Biochemistry & Molecular Biology

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

JP Schouten et al.

NUCLEIC ACIDS RESEARCH (2002)