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Volumn 96, Issue 2, 2012, Pages 176-189

Genetics of human enteric neuropathies

Author keywords

Enteric nervous system; Enteric neuropathies; Gene mutations; Genetic counseling; Hirschsprung; Reparative therapy

Indexed keywords

ALLGROVE SYNDROME; CELL COUNT; CELL NUCLEUS INCLUSION BODY; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CLINICAL FEATURE; ENTERIC NEUROPATHY; ESOPHAGUS ACHALASIA; GALACTOSIALIDOSIS; GANGLION; GANGLIONEUROMA; GENETIC COUNSELING; GENETIC DISORDER; GENETIC SCREENING; GENETICS; GOLDBERG SHPRINTZEN SYNDROME; HADDAD SYNDROME; HIRSCHSPRUNG DISEASE; HUMAN; INHERITANCE; INTESTINAL NEURONAL DYSPLASIA; INTESTINE INNERVATION; MOWAT WILSON SYNDROME; MULTIPLE ENDOCRINE NEOPLASIA; NERVE CELL; NERVOUS SYSTEM DEVELOPMENT; NEUROBLASTOMA; NEUROFIBROMATOSIS; NEURONAL INTRANUCLEAR INCLUSION DISEASE; NEUROPATHY; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; REVIEW; TRISOMY 21; VELOCARDIOFACIAL SYNDROME; WAARDENBURG SHAH SYNDROME; WAARDENBURG SYNDROME; WILSON DISEASE;

EID: 84856998426     PISSN: 03010082     EISSN: 18735118     Source Type: Journal    
DOI: 10.1016/j.pneurobio.2012.01.001     Document Type: Review
Times cited : (37)

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