Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity

Journal of Human Genetics

Volumn 52, Issue 11, 2007, Pages 907-914

  Maeda, Kouji ^a   Kaji, Ryuji ^a   Yasuno, Katsuhito ^b,c   Jambaldorj, Jamiyansuren ^a   Nodera, Hiroyuki ^a   Takashima, Hiroshi ^d   Nakagawa, Masanori ^e   Makino, Satoshi ^a   Tamiya, Gen ^a  

^a UNIVERSITY OF TOKUSHIMA   (Japan)

^b TOKAI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^d KAGOSHIMA UNIVERSITY   (Japan)

^e KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

Author keywords

Amyotrophic lateral sclerosis (ALS); Charcot Marie Tooth disease (CMT2P); Hereditary motor and sensory neuropathy with proximal dominancy (HMSN P); Hereditary motor neuropathy (HMN); Limb girdle muscular dystrophy (LGMD); Spinal muscular atrophy (SMA)

Indexed keywords

ADULT; ALLELE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENETIC HETEROGENEITY; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; JAPAN; MALE; MICROSATELLITE MARKER;

BASE SEQUENCE; DNA PRIMERS; FEMALE; GENES, DOMINANT; GENETIC HETEROGENEITY; HAPLOTYPES; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE;

EID: 36148948609     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-007-0193-7     Document Type: Article

References (9)

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