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Neurogenetics

Volumn 10, Issue 4, 2009, Pages 359-361

A novel de novo MFN2 mutation causing CMT2A with upper motor neuron signs

(7) Ajroud Driss, S a Fecto, F a Ajroud, K a Yang, Y a Donkervoort, S a Siddique, N a Siddique, T a

a NORTHWESTERN UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; MFN2 PROTEIN, HUMAN; MITOCHONDRIAL PROTEIN;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMAL; ARTICLE; CASE REPORT; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOLECULAR GENETICS; MOTOR NEURON DISEASE; MUTATION; PATHOPHYSIOLOGY; SEQUENCE ALIGNMENT;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; HUMANS; MALE; MEMBRANE PROTEINS; MITOCHONDRIAL PROTEINS; MOLECULAR SEQUENCE DATA; MOTOR NEURON DISEASE; MUTATION; SEQUENCE ALIGNMENT;

EID: 79958135857 PISSN: 13646745 EISSN: 13646753 Source Type: Journal
DOI: 10.1007/s10048-009-0188-y Document Type: Article

Times cited : (14)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.